Pending: 32006D0473

8.7.2006 EN Official Journal of the European Union L 187/35
(1) In order to permit the introduction of fruits ofCitrusL.,FortunellaSwingle,PoncirusRaf., and their hybrids from third countries into the Community or their movement within the Community under Directive 2000/29/EC, Commission Decision 98/83/EC of 8 January 1998 recognising certain third countries and certain areas of third countries as being free ofXanthomonas campestris(all strains pathogenic to Citrus),Cercospora angolensisCarv. et Mendes andGuignardia citricarpa Kiely(all strains pathogenic to Citrus)(2)recognised certain third countries and certain areas of third countries as being free from those harmful organisms.
(2) Since its adoption, Decision 98/83/EC has been amended several times. In the interest of clarity and rationality Decision 98/83/EC should, therefore, be repealed and replaced.
(3) New Zealand has submitted official information showing that its territory is free fromXanthomonas campestrisandGuignardia citricarpa. New Zealand should therefore be recognised as being free from those harmful organisms.
(4) South Africa has submitted official information showing that the magisterial districts of Hartswater and Warrenton in Northern Cape are free fromGuignardia citricarpa. These districts of South Africa should therefore be recognised as being free from this harmful organism.
(5) Australia has submitted information indicating that Queensland is no longer free fromXanthomonas campestris. Queensland should therefore no longer be recognised as being free from that harmful organism.
(6) The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on Plant Health,
(a) all citrus-growing third countries in Europe, Algeria, Egypt, Israel, Libya, Morocco, Tunisia and Turkey;
(b) Africa: South Africa, Gambia, Ghana, Guinea, Kenya, Sudan, Swaziland and Zimbabwe;
(c) Central and South America and the Caribbean: the Bahamas, Belize, Chile, Colombia, Costa Rica, Cuba, Ecuador, Honduras, Jamaica, Mexico, Nicaragua, Peru, the Dominican Republic, Saint Lucia, El Salvador, Surinam and Venezuela;
(d) Oceania: New Zealand.
(a) Australia: New South Wales, South Australia and Victoria;
(b) Brazil, except the States of Rio Grande do Sul, Santa Catarina, Paraná, São Paulo, Minas Gerais and Mato Grosso do Sul;
(c) United States: Arizona, California, Guam, Hawaii, Louisiana, Northern Mariana Islands, Puerto Rico, American Samoa, Texas and the United States Virgin Islands;
(d) Uruguay, except the Departments of Salto, Rivera and Paysandu — north of River Chapicuy.
(a) all citrus-growing third countries in North, Central and South America, the Caribbean, Asia, except Yemen, Europe and Oceania;
(b) all citrus-growing third countries in Africa, except Angola, Cameroon, Central African Republic, Democratic Republic of Congo, Gabon, Guinea, Kenya, Mozambique, Nigeria, Uganda, Zambia and Zimbabwe.
(a) all citrus-growing third countries in North, Central and South America, except Argentina and Brazil, the Caribbean and Europe;
(b) all citrus-growing third countries in Asia, except Bhutan, China, Indonesia, Philippines and Taiwan;
(c) all citrus-growing third countries in Africa, except South Africa, Kenya, Mozambique, Swaziland, Zambia and Zimbabwe;
(d) all citrus-growing third countries in Oceania, except Australia and Vanuatu.
(a) South Africa: Western Cape; Northern Cape: magisterial districts of Hartswater and Warrenton;
(b) Australia: South Australia, Western Australia and Northern Territory;
(c) China: all areas, except Sichuan, Yunnan, Guangdong, Fujian and Zhejiang;
(d) Brazil: all areas, except the States of Rio de Janeiro, São Paulo and Rio Grande do Sul.
THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Council Directive 2000/29/EC of 8 May 2000 on protective measures against the introduction into the Community of organisms harmful to plants or plant products and against their spread within the Community(1), and in particular points 16.2, 16.3 and 16.4 of Section I of Part A of Annex IV thereof,
(1) In order to permit the introduction of fruits ofCitrusL.,FortunellaSwingle,PoncirusRaf., and their hybrids from third countries into the Community or their movement within the Community under Directive 2000/29/EC, Commission Decision 98/83/EC of 8 January 1998 recognising certain third countries and certain areas of third countries as being free ofXanthomonas campestris(all strains pathogenic to Citrus),Cercospora angolensisCarv. et Mendes andGuignardia citricarpa Kiely(all strains pathogenic to Citrus)(2)recognised certain third countries and certain areas of third countries as being free from those harmful organisms.
(2) Since its adoption, Decision 98/83/EC has been amended several times. In the interest of clarity and rationality Decision 98/83/EC should, therefore, be repealed and replaced.
(3) New Zealand has submitted official information showing that its territory is free fromXanthomonas campestrisandGuignardia citricarpa. New Zealand should therefore be recognised as being free from those harmful organisms.
(4) South Africa has submitted official information showing that the magisterial districts of Hartswater and Warrenton in Northern Cape are free fromGuignardia citricarpa. These districts of South Africa should therefore be recognised as being free from this harmful organism.
(5) Australia has submitted information indicating that Queensland is no longer free fromXanthomonas campestris. Queensland should therefore no longer be recognised as being free from that harmful organism.
(6) The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on Plant Health,
HAS ADOPTED THIS DECISION:

Article 1
1. For the purposes of point 16.2 of Section I of Part A of Annex IV, the following third countries are recognised as being free from all strains ofXanthomonas campestrispathogenic to Citrus:
(a)
all citrus-growing third countries in Europe, Algeria, Egypt, Israel, Libya, Morocco, Tunisia and Turkey;
(b)
Africa: South Africa, Gambia, Ghana, Guinea, Kenya, Sudan, Swaziland and Zimbabwe;
(c)
Central and South America and the Caribbean: the Bahamas, Belize, Chile, Colombia, Costa Rica, Cuba, Ecuador, Honduras, Jamaica, Mexico, Nicaragua, Peru, the Dominican Republic, Saint Lucia, El Salvador, Surinam and Venezuela;
(d)
Oceania: New Zealand.
2. For the purposes of point 16.2 of Section I of Part A of Annex IV, the following areas are recognised as being free from all strains ofXanthomonas campestrispathogenic to Citrus:
(a)
Australia: New South Wales, South Australia and Victoria;
(b)
Brazil, except the States of Rio Grande do Sul, Santa Catarina, Paraná, São Paulo, Minas Gerais and Mato Grosso do Sul;
(c)
United States: Arizona, California, Guam, Hawaii, Louisiana, Northern Mariana Islands, Puerto Rico, American Samoa, Texas and the United States Virgin Islands;
(d)
Uruguay, except the Departments of Salto, Rivera and Paysandu — north of River Chapicuy.

Article 2
For the purposes of point 16.3 of Section I of Part A of Annex IV, the following third countries are recognised as being free fromCercospora angolensisCarv. et Mendes:
(a)
all citrus-growing third countries in North, Central and South America, the Caribbean, Asia, except Yemen, Europe and Oceania;
(b)
all citrus-growing third countries in Africa, except Angola, Cameroon, Central African Republic, Democratic Republic of Congo, Gabon, Guinea, Kenya, Mozambique, Nigeria, Uganda, Zambia and Zimbabwe.

Article 3
1. For the purposes of point 16.4 of Section I of Part A of Annex IV, the following third countries are recognised as being free from all strains ofGuignardia citricarpaKiely pathogenic to Citrus:
(a)
all citrus-growing third countries in North, Central and South America, except Argentina and Brazil, the Caribbean and Europe;
(b)
all citrus-growing third countries in Asia, except Bhutan, China, Indonesia, Philippines and Taiwan;
(c)
all citrus-growing third countries in Africa, except South Africa, Kenya, Mozambique, Swaziland, Zambia and Zimbabwe;
(d)
all citrus-growing third countries in Oceania, except Australia and Vanuatu.
2. For the purposes of point 16.4 of Section I of Part A of Annex IV, the following areas are recognised as being free from all strains ofGuignardia citricicarpaKiely pathogenic to Citrus:
(a)
South Africa: Western Cape; Northern Cape: magisterial districts of Hartswater and Warrenton;
(b)
Australia: South Australia, Western Australia and Northern Territory;
(c)
China: all areas, except Sichuan, Yunnan, Guangdong, Fujian and Zhejiang;
(d)
Brazil: all areas, except the States of Rio de Janeiro, São Paulo and Rio Grande do Sul.

Article 4
Decision 98/83/EC shall be repealed.

Article 5
This Decision is addressed to the Member States.

THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Council Directive 2000/29/EC of 8 May 2000 on protective measures against the introduction into the Community of organisms harmful to plants or plant products and against their spread within the Community(1), and in particular points 16.2, 16.3 and 16.4 of Section I of Part A of Annex IV thereof,
(1) In order to permit the introduction of fruits ofCitrusL.,FortunellaSwingle,PoncirusRaf., and their hybrids from third countries into the Community or their movement within the Community under Directive 2000/29/EC, Commission Decision 98/83/EC of 8 January 1998 recognising certain third countries and certain areas of third countries as being free ofXanthomonas campestris(all strains pathogenic to Citrus),Cercospora angolensisCarv. et Mendes andGuignardia citricarpa Kiely(all strains pathogenic to Citrus)(2)recognised certain third countries and certain areas of third countries as being free from those harmful organisms.
(2) Since its adoption, Decision 98/83/EC has been amended several times. In the interest of clarity and rationality Decision 98/83/EC should, therefore, be repealed and replaced.
(3) New Zealand has submitted official information showing that its territory is free fromXanthomonas campestrisandGuignardia citricarpa. New Zealand should therefore be recognised as being free from those harmful organisms.
(4) South Africa has submitted official information showing that the magisterial districts of Hartswater and Warrenton in Northern Cape are free fromGuignardia citricarpa. These districts of South Africa should therefore be recognised as being free from this harmful organism.
(5) Australia has submitted information indicating that Queensland is no longer free fromXanthomonas campestris. Queensland should therefore no longer be recognised as being free from that harmful organism.
(6) The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on Plant Health,
HAS ADOPTED THIS DECISION:
1. For the purposes of point 16.2 of Section I of Part A of Annex IV, the following third countries are recognised as being free from all strains ofXanthomonas campestrispathogenic to Citrus:
(a)
all citrus-growing third countries in Europe, Algeria, Egypt, Israel, Libya, Morocco, Tunisia and Turkey;
(b)
Africa: South Africa, Gambia, Ghana, Guinea, Kenya, Sudan, Swaziland and Zimbabwe;
(c)
Central and South America and the Caribbean: the Bahamas, Belize, Chile, Colombia, Costa Rica, Cuba, Ecuador, Honduras, Jamaica, Mexico, Nicaragua, Peru, the Dominican Republic, Saint Lucia, El Salvador, Surinam and Venezuela;
(d)
Oceania: New Zealand.
2. For the purposes of point 16.2 of Section I of Part A of Annex IV, the following areas are recognised as being free from all strains ofXanthomonas campestrispathogenic to Citrus:
(a)
Australia: New South Wales, South Australia and Victoria;
(b)
Brazil, except the States of Rio Grande do Sul, Santa Catarina, Paraná, São Paulo, Minas Gerais and Mato Grosso do Sul;
(c)
United States: Arizona, California, Guam, Hawaii, Louisiana, Northern Mariana Islands, Puerto Rico, American Samoa, Texas and the United States Virgin Islands;
(d)
Uruguay, except the Departments of Salto, Rivera and Paysandu — north of River Chapicuy.
For the purposes of point 16.3 of Section I of Part A of Annex IV, the following third countries are recognised as being free fromCercospora angolensisCarv. et Mendes:
(a)
all citrus-growing third countries in North, Central and South America, the Caribbean, Asia, except Yemen, Europe and Oceania;
(b)
all citrus-growing third countries in Africa, except Angola, Cameroon, Central African Republic, Democratic Republic of Congo, Gabon, Guinea, Kenya, Mozambique, Nigeria, Uganda, Zambia and Zimbabwe.
1. For the purposes of point 16.4 of Section I of Part A of Annex IV, the following third countries are recognised as being free from all strains ofGuignardia citricarpaKiely pathogenic to Citrus:
(a)
all citrus-growing third countries in North, Central and South America, except Argentina and Brazil, the Caribbean and Europe;
(b)
all citrus-growing third countries in Asia, except Bhutan, China, Indonesia, Philippines and Taiwan;
(c)
all citrus-growing third countries in Africa, except South Africa, Kenya, Mozambique, Swaziland, Zambia and Zimbabwe;
(d)
all citrus-growing third countries in Oceania, except Australia and Vanuatu.
2. For the purposes of point 16.4 of Section I of Part A of Annex IV, the following areas are recognised as being free from all strains ofGuignardia citricicarpaKiely pathogenic to Citrus:
(a)
South Africa: Western Cape; Northern Cape: magisterial districts of Hartswater and Warrenton;
(b)
Australia: South Australia, Western Australia and Northern Territory;
(c)
China: all areas, except Sichuan, Yunnan, Guangdong, Fujian and Zhejiang;
(d)
Brazil: all areas, except the States of Rio de Janeiro, São Paulo and Rio Grande do Sul.
Decision 98/83/EC shall be repealed.
This Decision is addressed to the Member States.

Pending: 32006D0241

25.3.2006 EN Official Journal of the European Union L 88/63
(1) Commission Decision 97/517/EC of 1 August 1997 concerning certain protective measures with regard to certain products of animal origin, excluding fishery products, originating in Madagascar(2)has been substantially amended(3). In the interests of clarity and rationality the said Decision should be codified.
(2) Community inspections in Madagascar have shown that there are serious deficiencies with regard to infrastructure and hygiene in meat establishments and that there are not enough guarantees of the efficiency of the controls carried out by the competent authorities. Animal health management in Madagascar shows severe deficiencies and non-application of Community rules. There is a potential risk for public health with regard to the production and processing of animal products, excluding fishery products, in this country.
(3) Imports of products of animal origin, excluding fishery products, from Madagascar should not be allowed until it can be guaranteed that no more risk exists.
(4) The measures provided for in this Decision are in conformity with the opinion of the Standing Committee on the Food Chain and Animal Health,
Commission Decision 97/517/EC (OJ L 214, 6.8.1997, p. 54)
Commission Decision 97/553/EC (OJ L 228, 19.8.1997, p. 31) Only as regards the reference to Decision 97/517/EC in Article 1
Decision 97/517/EC This Decision
Article 1 Article 1
Article 2 first paragraph Article 2
Article 2 second paragraph —
Article 3 —
— Article 3
Article 4 —
Article 5 Article 4
— Annex I
— Annex II
THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Council Directive 97/78/EC of 18 December 1997 laying down the principles governing the organisation of veterinary checks on products entering the Community from third countries(1), and in particular Article 22 thereof,
(1) Commission Decision 97/517/EC of 1 August 1997 concerning certain protective measures with regard to certain products of animal origin, excluding fishery products, originating in Madagascar(2)has been substantially amended(3). In the interests of clarity and rationality the said Decision should be codified.
(2) Community inspections in Madagascar have shown that there are serious deficiencies with regard to infrastructure and hygiene in meat establishments and that there are not enough guarantees of the efficiency of the controls carried out by the competent authorities. Animal health management in Madagascar shows severe deficiencies and non-application of Community rules. There is a potential risk for public health with regard to the production and processing of animal products, excluding fishery products, in this country.
(3) Imports of products of animal origin, excluding fishery products, from Madagascar should not be allowed until it can be guaranteed that no more risk exists.
(4) The measures provided for in this Decision are in conformity with the opinion of the Standing Committee on the Food Chain and Animal Health,
HAS ADOPTED THIS DECISION:

Article 1
This Decision shall apply to products of animal origin, excluding fishery products, originating in Madagascar.

Article 2
Member States shall prohibit imports of the products referred to in Article 1.

Article 3
Decision 97/517/EC is repealed.
References to the repealed Decision shall be construed as references to this Decision and shall be read in accordance with the correlation table in Annex II.

Article 4
This Decision is addressed to the Member States.

THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Council Directive 97/78/EC of 18 December 1997 laying down the principles governing the organisation of veterinary checks on products entering the Community from third countries(1), and in particular Article 22 thereof,
(1) Commission Decision 97/517/EC of 1 August 1997 concerning certain protective measures with regard to certain products of animal origin, excluding fishery products, originating in Madagascar(2)has been substantially amended(3). In the interests of clarity and rationality the said Decision should be codified.
(2) Community inspections in Madagascar have shown that there are serious deficiencies with regard to infrastructure and hygiene in meat establishments and that there are not enough guarantees of the efficiency of the controls carried out by the competent authorities. Animal health management in Madagascar shows severe deficiencies and non-application of Community rules. There is a potential risk for public health with regard to the production and processing of animal products, excluding fishery products, in this country.
(3) Imports of products of animal origin, excluding fishery products, from Madagascar should not be allowed until it can be guaranteed that no more risk exists.
(4) The measures provided for in this Decision are in conformity with the opinion of the Standing Committee on the Food Chain and Animal Health,
HAS ADOPTED THIS DECISION:
This Decision shall apply to products of animal origin, excluding fishery products, originating in Madagascar.
Member States shall prohibit imports of the products referred to in Article 1.
Decision 97/517/EC is repealed.
References to the repealed Decision shall be construed as references to this Decision and shall be read in accordance with the correlation table in Annex II.
This Decision is addressed to the Member States.
ANNEX IRepealed Decision and its amendment
Commission Decision 97/517/EC (OJ L 214, 6.8.1997, p. 54) |
Commission Decision 97/553/EC (OJ L 228, 19.8.1997, p. 31) | Only as regards the reference to Decision 97/517/EC in Article 1
ANNEX IICorrelation table
Decision 97/517/EC | This Decision
Article 1 | Article 1
Article 2 first paragraph | Article 2
Article 2 second paragraph | —
Article 3 | —
— | Article 3
Article 4 | —
Article 5 | Article 4
— | Annex I
— | Annex II

Pending: 32006D0135

23.2.2006 EN Official Journal of the European Union L 52/41
(1) Avian influenza is an infectious viral disease in poultry and birds, causing mortality and disturbances which can quickly take epizootic proportions liable to present a serious threat to animal health and to reduce sharply the profitability of poultry farming. Under certain circumstances the disease may also pose a risk to human health. There is a risk that the disease agent might be spread to other holdings, to wild birds and from one Member State to other Member States and third countries through the international trade in live birds or their products.
(2) Highly pathogenic avian influenza A virus of subtype H5N1 has been isolated from wild birds in certain parts of the Community and in third countries adjacent to the Community or populated by migratory birds during winter. The likelihood of virus introduction with wild birds is increasing during the forthcoming migratory season.
(3) Where an H5 avian influenza virus collected from poultry is isolated on the territory of a Member State and where, pending the determination of the neuraminidase (N) type or of the pathogenicity index, the clinical picture and the epidemiological circumstances justify the suspicion of highly pathogenic avian influenza caused by highly pathogenic influenza A virus of subtype H5N1 or the presence of highly pathogenic avian influenza, in particular of that subtype, has been confirmed, the affected Member State should apply certain protection measures to minimise the risk of disease spread.
(4) These protective measures should be implemented in addition to those foreseen in the framework of Council Directive 92/40/EEC of 19 May 1992 introducing Community measures for the control of avian influenza(5).
(5) However, the measures provided for in Directive 92/40/EEC are minimum control measures and require supplementary provisions notably on the movement of certain birds and of products from poultry and other birds originating in the zone affected by the disease.
(6) Given the particular disease risk and the epidemiological situation with regard to highly pathogenic avian influenza and taking into account the severe economic impact the disease may have, in particular when occurring in Densely Populated Poultry Areas, supplementary measures should aim at reinforcing the local control measures, regionalising the affected Member State by separating the affected part of the territory from the disease free part thereof, and providing reassurance to the poultry sector and the trade partners about the safety of products dispatched from the disease free part of the country.
(7) Taking account of the differences in disease risk in case of an outbreak of highly pathogenic avian influenza, a high risk area and a low risk area should be established by the affected Member State in close collaboration with the Commission.
(8) If the epidemiological situation so requires, measures appropriate in relation to the areas concerned by the outbreak or suspected outbreak of highly pathogenic avian influenza should be taken, in particular by describing these areas, and keeping this description updated depending on the situation, in Annex I to the present Decision in accordance with the procedure provided for in Article 10(3) or (4) of Directive 90/425/EEC and Article 9(3) or (4) of Directive 89/662/EEC.
(9) In the interests of consistency, it is appropriate to apply for the purposes of this Decision certain definitions provided for in Council Directive 2005/94/EC of 20 December 2005 on Community measures for the control of avian influenza and repealing Directive 92/40/EEC(6), Council Directive 90/539/EEC of 15 October 1990 on animal health conditions governing intra-Community trade in, and imports from third countries of, poultry and hatching eggs(7), Regulation (EC) No 853/2004 of the European Parliament and of the Council of 29 April 2004 laying down specific hygiene rules for food of animal origin(8), Regulation (EC) No 998/2003 of the European Parliament and of the Council of 26 May 2003 on the animal health requirements applicable to the non-commercial movement of pet animals and amending Council Directive 92/65/EEC(9).
(10) The measures laid down in Commission Decision 2005/734/EC of 19 October 2005 laying down biosecurity measures to reduce the risk of transmission of highly pathogenic avian influenza caused by Influenza virus A subtype H5N1 from birds living in the wild to poultry and other captive birds and providing for an early detection system in areas at particular risk(10)should be implemented in the areas affected by the disease.
(11) Council Directive 92/65/EEC of 13 July 1992 laying down animal health requirements governing trade in and imports into the Community of animals, semen, ova and embryos not subject to animal health requirements laid down in specific Community rules referred to in Annex A (I) to Directive 90/425/EEC(11)provides for approved bodies, institutes and centres and a model certificate to accompany animals or their gametes between such approved premises in different Member States. A derogation from the transport restrictions should be envisaged for birds coming from and proceeding to bodies, institutes and centres approved in accordance with that Directive.
(12) Transport of hatching eggs from the protection zones should be permitted under certain conditions. The dispatch of hatching eggs to other countries may be permitted subject in particular to compliance with the conditions referred to in Directive 2005/94/EC. In such cases the animal health certificates provided for in accordance with Directive 90/539/EEC should include a reference to this Decision.
(13) The dispatch from protection zones of meat, minced meat, meat preparations and meat products should be permitted subject to certain conditions, in particular as regards compliance with certain requirements of Regulation (EC) No 853/2004 and of Regulation (EC) No 854/2004 of the European Parliament and of the Council of 29 April 2004 laying down specific rules for the organisation of official controls on products of animal origin intended for human consumption(12).
(14) Council Directive 2002/99/EC of 16 December 2002 laying down the animal health rules governing the production, processing, distribution and introduction of products of animal origin for human consumption(13)establishes a list of treatments rendering meat from restricted areas safe, provides for the possibility to establish a specific identification mark and sets up the identification mark required for meat not authorised for placing on the market for animal health reasons. It is appropriate to permit the dispatch from the protection zones of meat bearing the health mark provided for in that Directive and meat products subjected to treatment referred to therein.
(15) Regulation (EC) No 1774/2002 of the European Parliament and of the Council of 3 October 2002 laying down health rules concerning animal by-products not intended for human consumption(14)authorises the placing on the market of a range of animal by-products, such as gelatine for technical use, materials for pharmaceutical use and others, originating in areas of the Community under animal health restrictions, because those products are considered safe due to the specific conditions of production, processing and utilisation that effectively inactivate possible pathogens or prevent contact with susceptible animals.
(16) This Decision should be reviewed in the light of the transposition of Directive 2005/94/EC by Member States.
(17) Given the disease risk, protection measures should be adopted at Community level in order to address the particular risks in different areas.
(18) The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health,
(a) ‘hatching eggs’ means eggs as defined in Article 2(2) of Directive 90/539/EEC;
(b) ‘wild feathered game’ means game as defined in point 1.5, second indent, and point 1.7 of Annex I to Regulation (EC) No 853/2004;
(c) ‘other captive birds’ means birds as defined in point 6 of Article 2 of Directive 2005/94/EC, including:(i)pet animals of the bird species as referred to in Article 3(a) of Regulation (EC) No 998/2003, and(ii)birds destined for approved bodies, institutes or centres as defined in Article 2(1) (c) of Directive 92/65/EEC. (i) pet animals of the bird species as referred to in Article 3(a) of Regulation (EC) No 998/2003, and (ii) birds destined for approved bodies, institutes or centres as defined in Article 2(1) (c) of Directive 92/65/EEC.
(i) pet animals of the bird species as referred to in Article 3(a) of Regulation (EC) No 998/2003, and
(ii) birds destined for approved bodies, institutes or centres as defined in Article 2(1) (c) of Directive 92/65/EEC.
(i) pet animals of the bird species as referred to in Article 3(a) of Regulation (EC) No 998/2003, and
(ii) birds destined for approved bodies, institutes or centres as defined in Article 2(1) (c) of Directive 92/65/EEC.
(a) The area listed in Part A of Annex I, hereinafter ‘area A’, shall be considered the area at higher risk including, but not limited to, the protection zone established in accordance with paragraphs 2 and 3 of Article 9 and the surveillance zones established in accordance paragraph 4 of Article 9 of Directive 92/40/EEC.
(b) The area listed in Part B of Annex I, hereinafter ‘area B’, shall separate area A from the disease free part of the affected Member State, if such part is identified, and the risk of disease in this area shall be considered minimal.
(a) notify the Commission and the other Member States,
(b) apply the measures provided for in Article 3(1) and (2) for as long as is necessary having regard to the geographical, administrative, ecological and epizootiological factors relating to avian influenza until the date indicated in Annex I and in any case for at least 21 days in the case of the protection zone and 30 days in the case of the surveillance zone after the date of completion of the preliminary cleansing and disinfection on the outbreak holding in accordance with Article 11 of Directive 92/40/EEC,
(c) keep the Commission and the other Member States informed about any development with regard to those areas.
(a) dispatched from areas A and B to other Member States and to third countries;
(b) dispatched from areas A and B to the remaining part of the national territory of the affected Member State;
(c) transported within areas A and B; and
(d) moved between areas A and B.
(a) dispatched from areas A and B to other Member States and to third countries;
(b) dispatched from areas A and B to the remaining part of the national territory of the affected Member State; and
(c) transported between areas A and B.
(a) from holdings in the protection zone for immediate slaughter to a slaughterhouse preferably located in the protection zone, if that is not possible, to a slaughterhouse outside the protection zone in the affected Member State which is designated by the competent authority;
(b) from holdings in the surveillance zone, during the 15 days following the establishment of the zone, directly to a slaughterhouse within or outside the surveillance zone in the affected Member State which is designated by the competent authority;
(c) from holdings in area A situated either within the surveillance zone after 15 days following its establishment or outside the surveillance zone, or in area B, to slaughterhouses in the affected Member State designated by the competent authority;
(d) from holdings situated outside the area A or area B for immediate slaughter in a slaughterhouse designated by the competent authority and situated in area A or area B;
(e) from holdings situated outside the area A or area B in transit by major highways or railways through area A outside the protection zone or area B.
(a) from a hatchery situated in the protection zone to a holding within the protection or surveillance zone at which there are no other poultry and which is placed under the official control provided for in Article 8(2) of Directive 92/40/EEC;
(b) from a hatchery situated in the surveillance zone to a holding or shed of such holding in the same Member State provided that appropriate biosecurity measures are applied and the holding is placed under official surveillance following the transport and day-old chicks shall remain on the holding of destination for at least 21 days;
(c) from a hatchery situated in area A in the surveillance zone to any holding provided, they are hatched from eggs collected from holdings situated outside the protection and surveillance zone, and that the hatchery can ensure by its logistics and biosecurity working conditions that no contact has occurred between these eggs and any other hatching eggs or day-old-chicks originating from poultry flocks within those zones and which are therefore of a different health status;
(d) from a hatchery situated in the part of area A outside the surveillance zone or in area B, and at least 10 km away from any suspected or infected hatchery or holding, to holdings under official control in the affected Member State;
(e) from a hatchery situated in the part of area A outside the protection zone or in area B to holdings within or outside the area A, provided that the day-old chicks are hatched from eggs complying with the requirements in Article 5(1)(d).
(a) from holdings in the protection zone to a holding within the surveillance zone at which there are no other poultry and which is placed under the official control provided for in Article 8(2) of Directive 92/40/EEC;
(b) from holdings in the surveillance zone after the 15 days following its establishment to a holding in which there is no other poultry in the same Member State; that holding shall be placed under official surveillance following the arrival of the ready-to-lay poultry and the ready-to-lay poultry shall remain on the holding of destination for at least 21 days;
(c) from holdings situated in the part of area A outside the surveillance zone or area B, and at least 10 km away from any suspected holding, to holdings under official control in the affected Member State.
(a) collected on holdings situated on the day of collection in the protection zone to a hatchery designated by the competent authority; provided the eggs and their packing are disinfected before dispatch;
(b) collected in holdings situated on the day of collection in the surveillance zone to a hatchery in the affected Member State which is designated by the competent authority, provided the eggs and their packaging are disinfected before dispatch;
(c) collected in holdings situated on the day of collection in area A outside the surveillance zone or area B, and at least 10 km away from any suspect holding, to a designated hatchery in the affected Member State, or following agreement between the competent authorities, to a designated hatchery in another Member State or third country;
(d) collected from holdings in area A outside the protection or surveillance zone or in area B on which the poultry has tested negative in a serological survey for avian influenza capable of detecting 5 % prevalence of disease with at least a 95 % level of confidence and traceability is ensured, to hatcheries within or outside the areas A or B.
(a) fresh meat from poultry, including meat from ratites, referred to in Article 4(1) (a) and (b) if such meat is marked with the identification mark provided for in Annex II to Directive 2002/99/EC and is intended for transport to an establishment for treatment as required for avian influenza in table 1(a), (b) or (c) of Annex III to that Directive;
(b) fresh meat from poultry, including meat from ratites, originating in area A, outside the protection zone and the surveillance zones during 15 days following its establishment, or area B, or produced from poultry referred to in Article 4(1)(d) and produced in accordance with Annex II and Sections II and III of Annex III to Regulation (EC) No 853/2004 and controlled in accordance with Sections I, II, III, and Chapters V and VII of Section IV of Annex I to Regulation (EC) No 854/2004;
(c) minced meat, meat preparations, mechanically separated meat and meat products containing meat referred to in point (b) and produced in accordance with Sections V and VI of Annex III to Regulation (EC) No 853/2004;
(d) fresh meat from poultry and farmed feathered game, minced meat and meat preparations and mechanically separated meat containing such meat, obtained from slaughter poultry or farmed feathered game originating in the part of area A outside the protection zone from area A or area B into the remaining part of its national territory of, if such meat:(i)was identified with a round stamp as setup in accordance with Article 4(2) of Directive 2002/99/EC in Annex IV to the present Decision; and(ii)was obtained, cut, stored and transported separately from other fresh meat from poultry or farmed feathered game destined for dispatch to other Member States or for exports to third countries; and(iii)is used in such a way as to avoid it being introduced into meat products or meat preparations intended for placing on the market in other Member States or for export to third countries, unless it has undergone the treatment as required for avian influenza specified in table 1(a), (b) or (c) of Annex III to Directive 2002/99/EC. (i) was identified with a round stamp as setup in accordance with Article 4(2) of Directive 2002/99/EC in Annex IV to the present Decision; and (ii) was obtained, cut, stored and transported separately from other fresh meat from poultry or farmed feathered game destined for dispatch to other Member States or for exports to third countries; and (iii) is used in such a way as to avoid it being introduced into meat products or meat preparations intended for placing on the market in other Member States or for export to third countries, unless it has undergone the treatment as required for avian influenza specified in table 1(a), (b) or (c) of Annex III to Directive 2002/99/EC.
(i) was identified with a round stamp as setup in accordance with Article 4(2) of Directive 2002/99/EC in Annex IV to the present Decision; and
(ii) was obtained, cut, stored and transported separately from other fresh meat from poultry or farmed feathered game destined for dispatch to other Member States or for exports to third countries; and
(iii) is used in such a way as to avoid it being introduced into meat products or meat preparations intended for placing on the market in other Member States or for export to third countries, unless it has undergone the treatment as required for avian influenza specified in table 1(a), (b) or (c) of Annex III to Directive 2002/99/EC.
(i) was identified with a round stamp as setup in accordance with Article 4(2) of Directive 2002/99/EC in Annex IV to the present Decision; and
(ii) was obtained, cut, stored and transported separately from other fresh meat from poultry or farmed feathered game destined for dispatch to other Member States or for exports to third countries; and
(iii) is used in such a way as to avoid it being introduced into meat products or meat preparations intended for placing on the market in other Member States or for export to third countries, unless it has undergone the treatment as required for avian influenza specified in table 1(a), (b) or (c) of Annex III to Directive 2002/99/EC.
(a) fresh meat from wild feathered game originating in area A or area B, if such meat is marked with the health mark provided for in Annex II to Directive 2002/99/EC and is intended for transport to an establishment for treatment as required for avian influenza in table 1(a), (b) or (c) of Annex III to that Directive;
(b) meat products produced from meat from wild feathered game originating in area A or in area B which were subjected to a treatment as required for avian influenza in table 1(a), (b) or (c) of Annex III to Directive 2002/99/EC;
(c) fresh meat from wild feathered game originating outside the areas A and B and produced in establishments within area A or area B in accordance with Section IV of Annex III to Regulation (EC) No 853/2004 and controlled in accordance with Chapter VIII of Section IV of Annex I to Regulation (EC) No 854/2004;
(d) minced meat, meat preparations, mechanically separated meat and meat products containing meat referred to in point (c) and produced in establishments situated in area A or area B in accordance with Sections V and VI of Annex III to Regulation (EC) No 853/2004.
(a) for human consumption to a packing centre designated by the competent authority, provided that they are packed in disposable packaging and that all biosecurity measures required by the competent authority are applied;
(b) to an establishment for the manufacture of egg products as set out in Chapter II of Section X of Annex III to Regulation (EC) No 853/2004 to be handled and treated in accordance with Chapter XI of Annex II to Regulation (EC) No 852/2004;
(c) for disposal in accordance with Regulation (EC) No 1774/2002.
(a) eggs for human consumption collected from holdings in area A, outside the protection or surveillance zone, or area B;
(b) pasteurised egg products in accordance with Chapter II of Section X of Annex III to Regulation (EC) No 853/2004.
(a) the dispatch from area A or area B of the animal by products complying with the conditions set up in Chapters II (A), III (B), IV (A), VI (A and B), VII (A), VIII (A), IX (A)and X (A) of Annex VII, and Chapters II (B), III (II) (A) and VII (A) (1)(a) of Annex VIII to Regulation (EC) No 1774/2002;
(b) the dispatch from area B of untreated feathers or parts of feathers in accordance with Chapter VIII (A) (1) (a) of Annex VIII to Regulation (EC) No 1774/2002, produced from poultry or farmed feathered game;
(c) the dispatch from area A or area B of feathers and parts of feathers that have been treated with a steam current, or by some other method that ensures that no pathogens remains, produced from poultry or farmed feathered game.
ISO Country Code Member State Area A Date until applicable
ISO Country Code Member State Area B Date until applicable
Dimensions:XYZ(1)= 8 mm1234(2)= 11 mmCircle outer diameter= not less than 30 mmLine thickness of circle= 3 mm Dimensions:XYZ(1)= 8 mm1234(2)= 11 mmCircle outer diameter= not less than 30 mmLine thickness of circle= 3 mm
Dimensions:XYZ(1)= 8 mm1234(2)= 11 mmCircle outer diameter= not less than 30 mmLine thickness of circle= 3 mm
Dimensions:XYZ(1)= 8 mm1234(2)= 11 mmCircle outer diameter= not less than 30 mmLine thickness of circle= 3 mm
THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to Council Directive 89/662/EEC of 11 December 1989 concerning veterinary checks in intra-Community trade with a view to the completion of the internal market(1), and in particular Article 9(4) thereof,
Having regard to Council Directive 90/425/EEC of 26 June 1990 concerning veterinary and zootechnical checks applicable in intra-Community trade in certain live animals and products with a view to the completion of the internal market(2), and in particular Article 10(4) thereof,
Having regard to Regulation (EC) No 998/2003 of 26 May 2003 of the European Parliament and of the Council on the animal health requirements applicable to the non-commercial movement of pet animals and amending Council Directive 92/65/EEC(3), and in particular Article 18 thereof,
Having regard to Council Directive 2005/94/EC of 20 December 2005 on Community measures for the control of avian influenza and repealing Directive 92/40/EEC(4), and in particular Article 66(2) thereof,
(1) Avian influenza is an infectious viral disease in poultry and birds, causing mortality and disturbances which can quickly take epizootic proportions liable to present a serious threat to animal health and to reduce sharply the profitability of poultry farming. Under certain circumstances the disease may also pose a risk to human health. There is a risk that the disease agent might be spread to other holdings, to wild birds and from one Member State to other Member States and third countries through the international trade in live birds or their products.
(2) Highly pathogenic avian influenza A virus of subtype H5N1 has been isolated from wild birds in certain parts of the Community and in third countries adjacent to the Community or populated by migratory birds during winter. The likelihood of virus introduction with wild birds is increasing during the forthcoming migratory season.
(3) Where an H5 avian influenza virus collected from poultry is isolated on the territory of a Member State and where, pending the determination of the neuraminidase (N) type or of the pathogenicity index, the clinical picture and the epidemiological circumstances justify the suspicion of highly pathogenic avian influenza caused by highly pathogenic influenza A virus of subtype H5N1 or the presence of highly pathogenic avian influenza, in particular of that subtype, has been confirmed, the affected Member State should apply certain protection measures to minimise the risk of disease spread.
(4) These protective measures should be implemented in addition to those foreseen in the framework of Council Directive 92/40/EEC of 19 May 1992 introducing Community measures for the control of avian influenza(5).
(5) However, the measures provided for in Directive 92/40/EEC are minimum control measures and require supplementary provisions notably on the movement of certain birds and of products from poultry and other birds originating in the zone affected by the disease.
(6) Given the particular disease risk and the epidemiological situation with regard to highly pathogenic avian influenza and taking into account the severe economic impact the disease may have, in particular when occurring in Densely Populated Poultry Areas, supplementary measures should aim at reinforcing the local control measures, regionalising the affected Member State by separating the affected part of the territory from the disease free part thereof, and providing reassurance to the poultry sector and the trade partners about the safety of products dispatched from the disease free part of the country.
(7) Taking account of the differences in disease risk in case of an outbreak of highly pathogenic avian influenza, a high risk area and a low risk area should be established by the affected Member State in close collaboration with the Commission.
(8) If the epidemiological situation so requires, measures appropriate in relation to the areas concerned by the outbreak or suspected outbreak of highly pathogenic avian influenza should be taken, in particular by describing these areas, and keeping this description updated depending on the situation, in Annex I to the present Decision in accordance with the procedure provided for in Article 10(3) or (4) of Directive 90/425/EEC and Article 9(3) or (4) of Directive 89/662/EEC.
(9) In the interests of consistency, it is appropriate to apply for the purposes of this Decision certain definitions provided for in Council Directive 2005/94/EC of 20 December 2005 on Community measures for the control of avian influenza and repealing Directive 92/40/EEC(6), Council Directive 90/539/EEC of 15 October 1990 on animal health conditions governing intra-Community trade in, and imports from third countries of, poultry and hatching eggs(7), Regulation (EC) No 853/2004 of the European Parliament and of the Council of 29 April 2004 laying down specific hygiene rules for food of animal origin(8), Regulation (EC) No 998/2003 of the European Parliament and of the Council of 26 May 2003 on the animal health requirements applicable to the non-commercial movement of pet animals and amending Council Directive 92/65/EEC(9).
(10) The measures laid down in Commission Decision 2005/734/EC of 19 October 2005 laying down biosecurity measures to reduce the risk of transmission of highly pathogenic avian influenza caused by Influenza virus A subtype H5N1 from birds living in the wild to poultry and other captive birds and providing for an early detection system in areas at particular risk(10)should be implemented in the areas affected by the disease.
(11) Council Directive 92/65/EEC of 13 July 1992 laying down animal health requirements governing trade in and imports into the Community of animals, semen, ova and embryos not subject to animal health requirements laid down in specific Community rules referred to in Annex A (I) to Directive 90/425/EEC(11)provides for approved bodies, institutes and centres and a model certificate to accompany animals or their gametes between such approved premises in different Member States. A derogation from the transport restrictions should be envisaged for birds coming from and proceeding to bodies, institutes and centres approved in accordance with that Directive.
(12) Transport of hatching eggs from the protection zones should be permitted under certain conditions. The dispatch of hatching eggs to other countries may be permitted subject in particular to compliance with the conditions referred to in Directive 2005/94/EC. In such cases the animal health certificates provided for in accordance with Directive 90/539/EEC should include a reference to this Decision.
(13) The dispatch from protection zones of meat, minced meat, meat preparations and meat products should be permitted subject to certain conditions, in particular as regards compliance with certain requirements of Regulation (EC) No 853/2004 and of Regulation (EC) No 854/2004 of the European Parliament and of the Council of 29 April 2004 laying down specific rules for the organisation of official controls on products of animal origin intended for human consumption(12).
(14) Council Directive 2002/99/EC of 16 December 2002 laying down the animal health rules governing the production, processing, distribution and introduction of products of animal origin for human consumption(13)establishes a list of treatments rendering meat from restricted areas safe, provides for the possibility to establish a specific identification mark and sets up the identification mark required for meat not authorised for placing on the market for animal health reasons. It is appropriate to permit the dispatch from the protection zones of meat bearing the health mark provided for in that Directive and meat products subjected to treatment referred to therein.
(15) Regulation (EC) No 1774/2002 of the European Parliament and of the Council of 3 October 2002 laying down health rules concerning animal by-products not intended for human consumption(14)authorises the placing on the market of a range of animal by-products, such as gelatine for technical use, materials for pharmaceutical use and others, originating in areas of the Community under animal health restrictions, because those products are considered safe due to the specific conditions of production, processing and utilisation that effectively inactivate possible pathogens or prevent contact with susceptible animals.
(16) This Decision should be reviewed in the light of the transposition of Directive 2005/94/EC by Member States.
(17) Given the disease risk, protection measures should be adopted at Community level in order to address the particular risks in different areas.
(18) The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health,
HAS ADOPTED THIS DECISION:

Subject matter, scope and definitions
Article 1
1. This Decision lays down certain protection measures to be applied in cases of highly pathogenic avian influenza in poultry in the territory of a Member State (hereinafter the ‘affected Member State’), caused by influenza A virus of subtype H5 suspected (‘suspected outbreak’) or confirmed (‘outbreak’) to be of the neuraminidase type N1, in order to prevent the spread of avian influenza into the disease free parts of the Community through movement of poultry, other birds as well as products thereof.
2. Except as otherwise provided, the definitions of Directive 2005/94/EC shall apply. In addition, the following definitions shall apply:
(a)
‘hatching eggs’ means eggs as defined in Article 2(2) of Directive 90/539/EEC;
(b)
‘wild feathered game’ means game as defined in point 1.5, second indent, and point 1.7 of Annex I to Regulation (EC) No 853/2004;
(c)
‘other captive birds’ means birds as defined in point 6 of Article 2 of Directive 2005/94/EC, including:
(i)
pet animals of the bird species as referred to in Article 3(a) of Regulation (EC) No 998/2003, and
(ii)
birds destined for approved bodies, institutes or centres as defined in Article 2(1) (c) of Directive 92/65/EEC.
3. For the purpose of this Decision the following shall also apply:
(a)
The area listed in Part A of Annex I, hereinafter ‘area A’, shall be considered the area at higher risk including, but not limited to, the protection zone established in accordance with paragraphs 2 and 3 of Article 9 and the surveillance zones established in accordance paragraph 4 of Article 9 of Directive 92/40/EEC.
(b)
The area listed in Part B of Annex I, hereinafter ‘area B’, shall separate area A from the disease free part of the affected Member State, if such part is identified, and the risk of disease in this area shall be considered minimal.
4. The measures set down in this Decision shall be applied without prejudice to the measures to be applied in the event of an outbreak of avian influenza in poultry taken in accordance with Directive 92/40/EEC.

Establishment of areas A and B
Article 2
1. Immediately following an outbreak or suspected outbreak of highly pathogenic avian influenza caused by influenza A virus of subtype H5 suspected or confirmed to be of the neuraminidase type N1, the affected Member State shall establish areas A and B, having regard to the geographical, administrative, ecological and epizootiological factors relating to avian influenza, and notify them to the Commission, to the other Member States and, as appropriate, to the public.
2. The Commission, in collaboration with the affected Member State, shall examine the areas established by the affected Member State and take the appropriate measures in relation to those areas pursuant to Article 9(3) and (4) of Directive 89/662/EEC or to Article 10(3) or (4) of Directive 90/425/EEC.
3. If the neuraminidase type is confirmed as being different from N1, or the virus as of low pathogenicity, the affected Member State shall abolish the measures taken by it in relation to the areas concerned and notify the Commission and the other Member States.
The Commission, in collaboration with the affected Member State, shall take the appropriate measures pursuant to Article 9(3) or (4) of Directive 89/662/EEC and to Article 10(3) or (4) of Directive 90/425/EEC.
4. If the presence of a highly pathogenic influenza A virus, notably of the subtype H5N1, is confirmed in poultry, the affected Member States shall:
(a)
notify the Commission and the other Member States,
(b)
apply the measures provided for in Article 3(1) and (2) for as long as is necessary having regard to the geographical, administrative, ecological and epizootiological factors relating to avian influenza until the date indicated in Annex I and in any case for at least 21 days in the case of the protection zone and 30 days in the case of the surveillance zone after the date of completion of the preliminary cleansing and disinfection on the outbreak holding in accordance with Article 11 of Directive 92/40/EEC,
(c)
keep the Commission and the other Member States informed about any development with regard to those areas.
The Commission, in collaboration with the affected Member State, shall take the appropriate measures pursuant to Article 9(3) or (4) of Directive 89/662/EEC and to Article 10(3) or (4) of Directive 90/425/EEC.

General prohibition
Article 3
1. The affected Member State shall ensure that no live poultry and live birds other than poultry, and hatching eggs thereof are:
(a)
dispatched from areas A and B to other Member States and to third countries;
(b)
dispatched from areas A and B to the remaining part of the national territory of the affected Member State;
(c)
transported within areas A and B; and
(d)
moved between areas A and B.
2. The affected Member State shall ensure that no products other than hatching eggs of the species referred to in paragraph 1 and of wild feathered game are:
(a)
dispatched from areas A and B to other Member States and to third countries;
(b)
dispatched from areas A and B to the remaining part of the national territory of the affected Member State; and
(c)
transported between areas A and B.

Derogations for live birds and day-old chicks
Article 4
1. By way of derogation from Article 3(1), the affected Member State may authorise the transport of poultry or farmed feathered game, including spent laying hens,
(a)
from holdings in the protection zone for immediate slaughter to a slaughterhouse preferably located in the protection zone, if that is not possible, to a slaughterhouse outside the protection zone in the affected Member State which is designated by the competent authority;
(b)
from holdings in the surveillance zone, during the 15 days following the establishment of the zone, directly to a slaughterhouse within or outside the surveillance zone in the affected Member State which is designated by the competent authority;
(c)
from holdings in area A situated either within the surveillance zone after 15 days following its establishment or outside the surveillance zone, or in area B, to slaughterhouses in the affected Member State designated by the competent authority;
(d)
from holdings situated outside the area A or area B for immediate slaughter in a slaughterhouse designated by the competent authority and situated in area A or area B;
(e)
from holdings situated outside the area A or area B in transit by major highways or railways through area A outside the protection zone or area B.
2. By way of derogation from Article 3(1), the affected Member State may authorise the transport of day-old chicks:
(a)
from a hatchery situated in the protection zone to a holding within the protection or surveillance zone at which there are no other poultry and which is placed under the official control provided for in Article 8(2) of Directive 92/40/EEC;
(b)
from a hatchery situated in the surveillance zone to a holding or shed of such holding in the same Member State provided that appropriate biosecurity measures are applied and the holding is placed under official surveillance following the transport and day-old chicks shall remain on the holding of destination for at least 21 days;
(c)
from a hatchery situated in area A in the surveillance zone to any holding provided, they are hatched from eggs collected from holdings situated outside the protection and surveillance zone, and that the hatchery can ensure by its logistics and biosecurity working conditions that no contact has occurred between these eggs and any other hatching eggs or day-old-chicks originating from poultry flocks within those zones and which are therefore of a different health status;
(d)
from a hatchery situated in the part of area A outside the surveillance zone or in area B, and at least 10 km away from any suspected or infected hatchery or holding, to holdings under official control in the affected Member State;
(e)
from a hatchery situated in the part of area A outside the protection zone or in area B to holdings within or outside the area A, provided that the day-old chicks are hatched from eggs complying with the requirements in Article 5(1)(d).
3. By way of derogation from Article 3(1), the affected Member State may authorise the transport of ready-to-lay pullets, turkeys for fattening and other poultry or farmed feathered game:
(a)
from holdings in the protection zone to a holding within the surveillance zone at which there are no other poultry and which is placed under the official control provided for in Article 8(2) of Directive 92/40/EEC;
(b)
from holdings in the surveillance zone after the 15 days following its establishment to a holding in which there is no other poultry in the same Member State; that holding shall be placed under official surveillance following the arrival of the ready-to-lay poultry and the ready-to-lay poultry shall remain on the holding of destination for at least 21 days;
(c)
from holdings situated in the part of area A outside the surveillance zone or area B, and at least 10 km away from any suspected holding, to holdings under official control in the affected Member State.
4. By way of derogation from Article 3(1), the affected Member State may authorise transport of birds accompanying their owner to premises outside the area A or area B, if the consignment either consists of not more than 5 caged birds from holdings not keeping poultry or is destined for a quarantine established in accordance with Decision 2000/666/EC, and the birds are accompanied by a veterinary certificate in accordance with the model set up in Annex II, certifying compliance with the established animal health conditions, where required based on owners’ declaration in accordance with the model set up in Annex III.
5. The animal health certificates in accordance with Model 2 of Annex IV to Council Directive 90/539/EEC accompanying consignments of day-old chicks referred to in paragraph 2(c) and (e) shall include the words:
‘The consignment complies with the animal health conditions laid down in Commission Decision 2006/135/EC.’
6. Movements allowed in paragraphs 1(a), 2(a) and 3(a) shall be directly executed, under official control. They shall be authorised only after the official veterinarian has carried out a health inspection of the holding. The means of transport used must be cleaned and disinfected before and after use.

Derogations for hatching eggs
Article 5
1. By way of derogation from Article 3(1), the affected Member State may authorise the dispatch of hatching eggs:
(a)
collected on holdings situated on the day of collection in the protection zone to a hatchery designated by the competent authority; provided the eggs and their packing are disinfected before dispatch;
(b)
collected in holdings situated on the day of collection in the surveillance zone to a hatchery in the affected Member State which is designated by the competent authority, provided the eggs and their packaging are disinfected before dispatch;
(c)
collected in holdings situated on the day of collection in area A outside the surveillance zone or area B, and at least 10 km away from any suspect holding, to a designated hatchery in the affected Member State, or following agreement between the competent authorities, to a designated hatchery in another Member State or third country;
(d)
collected from holdings in area A outside the protection or surveillance zone or in area B on which the poultry has tested negative in a serological survey for avian influenza capable of detecting 5 % prevalence of disease with at least a 95 % level of confidence and traceability is ensured, to hatcheries within or outside the areas A or B.
2. Movements allowed in paragraph 1(a) shall be directly executed, under official control and only after the official veterinarian has carried out a health inspection of the holding and the means of transport are cleaned and disinfected before and after use.
3. The animal health certificates in accordance with Model 1 of Annex IV to Council Directive 90/539/EEC accompanying consignments of hatching eggs referred to in paragraph 1(c) and (d) to other Member States shall include the words:
‘The consignment complies with the animal health conditions laid down in Commission Decision 2006/135/EC.’

Derogations for meat, minced meat, meat preparations, mechanically separated meat and meat products
Article 6
1. By way of derogation from Article 3(2), the affected Member State shall authorise the dispatch of:
(a)
fresh meat from poultry, including meat from ratites, referred to in Article 4(1) (a) and (b) if such meat is marked with the identification mark provided for in Annex II to Directive 2002/99/EC and is intended for transport to an establishment for treatment as required for avian influenza in table 1(a), (b) or (c) of Annex III to that Directive;
(b)
fresh meat from poultry, including meat from ratites, originating in area A, outside the protection zone and the surveillance zones during 15 days following its establishment, or area B, or produced from poultry referred to in Article 4(1)(d) and produced in accordance with Annex II and Sections II and III of Annex III to Regulation (EC) No 853/2004 and controlled in accordance with Sections I, II, III, and Chapters V and VII of Section IV of Annex I to Regulation (EC) No 854/2004;
(c)
minced meat, meat preparations, mechanically separated meat and meat products containing meat referred to in point (b) and produced in accordance with Sections V and VI of Annex III to Regulation (EC) No 853/2004;
(d)
fresh meat from poultry and farmed feathered game, minced meat and meat preparations and mechanically separated meat containing such meat, obtained from slaughter poultry or farmed feathered game originating in the part of area A outside the protection zone from area A or area B into the remaining part of its national territory of, if such meat:
(i)
was identified with a round stamp as setup in accordance with Article 4(2) of Directive 2002/99/EC in Annex IV to the present Decision; and
(ii)
was obtained, cut, stored and transported separately from other fresh meat from poultry or farmed feathered game destined for dispatch to other Member States or for exports to third countries; and
(iii)
is used in such a way as to avoid it being introduced into meat products or meat preparations intended for placing on the market in other Member States or for export to third countries, unless it has undergone the treatment as required for avian influenza specified in table 1(a), (b) or (c) of Annex III to Directive 2002/99/EC.
2. By way of derogation from Article 3(2), the affected Member State shall authorise the dispatch of:
(a)
fresh meat from wild feathered game originating in area A or area B, if such meat is marked with the health mark provided for in Annex II to Directive 2002/99/EC and is intended for transport to an establishment for treatment as required for avian influenza in table 1(a), (b) or (c) of Annex III to that Directive;
(b)
meat products produced from meat from wild feathered game originating in area A or in area B which were subjected to a treatment as required for avian influenza in table 1(a), (b) or (c) of Annex III to Directive 2002/99/EC;
(c)
fresh meat from wild feathered game originating outside the areas A and B and produced in establishments within area A or area B in accordance with Section IV of Annex III to Regulation (EC) No 853/2004 and controlled in accordance with Chapter VIII of Section IV of Annex I to Regulation (EC) No 854/2004;
(d)
minced meat, meat preparations, mechanically separated meat and meat products containing meat referred to in point (c) and produced in establishments situated in area A or area B in accordance with Sections V and VI of Annex III to Regulation (EC) No 853/2004.
3. The affected Member State shall ensure that the products referred to in paragraphs 1(b), (c) and 2(b), (c), (d) are accompanied by commercial documents stating:
‘The consignment complies with the animal health conditions laid down in Commission Decision 2006/135/EC.’

Derogations for eggs for human consumption and egg products
Article 7
1. By way of derogation from Article 3(2), the affected Member State may authorise the dispatch of eggs collected from holdings in the protection or surveillance zone:
(a)
for human consumption to a packing centre designated by the competent authority, provided that they are packed in disposable packaging and that all biosecurity measures required by the competent authority are applied;
(b)
to an establishment for the manufacture of egg products as set out in Chapter II of Section X of Annex III to Regulation (EC) No 853/2004 to be handled and treated in accordance with Chapter XI of Annex II to Regulation (EC) No 852/2004;
(c)
for disposal in accordance with Regulation (EC) No 1774/2002.
2. By way of derogation from Article 3(2), the dispatch to any destination shall be allowed for:
(a)
eggs for human consumption collected from holdings in area A, outside the protection or surveillance zone, or area B;
(b)
pasteurised egg products in accordance with Chapter II of Section X of Annex III to Regulation (EC) No 853/2004.
3. The affected Member State shall ensure that consignments of eggs for human consumption referred to in paragraph 1(a) are accompanied by commercial documents stating:
‘The consignment complies with the animal health conditions laid down in Commission Decision 2006/135/EC.’

Derogation for animal by-products
Article 8
1. By way of derogation from Article 3(2), the affected Member State shall authorise:
(a)
the dispatch from area A or area B of the animal by products complying with the conditions set up in Chapters II (A), III (B), IV (A), VI (A and B), VII (A), VIII (A), IX (A)and X (A) of Annex VII, and Chapters II (B), III (II) (A) and VII (A) (1)(a) of Annex VIII to Regulation (EC) No 1774/2002;
(b)
the dispatch from area B of untreated feathers or parts of feathers in accordance with Chapter VIII (A) (1) (a) of Annex VIII to Regulation (EC) No 1774/2002, produced from poultry or farmed feathered game;
(c)
the dispatch from area A or area B of feathers and parts of feathers that have been treated with a steam current, or by some other method that ensures that no pathogens remains, produced from poultry or farmed feathered game.
2. The affected Member State shall ensure that the products referred to in paragraph 1(b) and (c) of this Article are accompanied by a commercial document in accordance with Chapter X of Annex II to Regulation (EC) No 1774/2002 stating, in the case of the products referred to in paragraph 1(c) of this Article, in point 6.1 of that document that those products have been treated with a steam current or by some other method ensuring that no pathogens remains.
However, that commercial document shall not be required for processed decorative feathers, processed feathers carried by travellers for their private use or consignments of processed feathers sent to private individuals for non-industrial purpose.

Conditions for movements
Article 9
1. Where movements of animals or products thereof covered by this Decision are authorised under Articles 4, 5, 6, 7 and 8, the authorisation shall be based on the favourable outcome of a risk assessment carried out by the competent authority and all appropriate biosecurity measures shall be taken to avoid the spread of avian influenza.
2. Where the dispatch, movement or transport of products referred to in paragraph 1 are authorised under Articles 5, 6, 7 and 8, subject to justified conditions or limitations, they must be obtained, handled, treated, stored and transported without compromising the animal health status of other products fulfilling all the animal health requirements for trade, placing on the market or export to third countries.

Compliance and Information
Article 10
All Member States shall immediately adopt and publish the measures necessary to comply with this Decision. They shall immediately inform the Commission thereof.
The affected Member State shall apply those measures as soon as it reasonably suspects the presence of highly pathogenic avian influenza virus, in particular of the subtype H5N1, in poultry.
The affected Member State shall regularly provide to the Commission and the other Member States the necessary information on the epidemiology of the disease and, where appropriate the additional control and surveillance measures and the awareness campaigns implemented.

Addressee
Article 11
This Decision is addressed to the Member States.

THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to Council Directive 89/662/EEC of 11 December 1989 concerning veterinary checks in intra-Community trade with a view to the completion of the internal market(1), and in particular Article 9(4) thereof,
Having regard to Council Directive 90/425/EEC of 26 June 1990 concerning veterinary and zootechnical checks applicable in intra-Community trade in certain live animals and products with a view to the completion of the internal market(2), and in particular Article 10(4) thereof,
Having regard to Regulation (EC) No 998/2003 of 26 May 2003 of the European Parliament and of the Council on the animal health requirements applicable to the non-commercial movement of pet animals and amending Council Directive 92/65/EEC(3), and in particular Article 18 thereof,
Having regard to Council Directive 2005/94/EC of 20 December 2005 on Community measures for the control of avian influenza and repealing Directive 92/40/EEC(4), and in particular Article 66(2) thereof,
(1) Avian influenza is an infectious viral disease in poultry and birds, causing mortality and disturbances which can quickly take epizootic proportions liable to present a serious threat to animal health and to reduce sharply the profitability of poultry farming. Under certain circumstances the disease may also pose a risk to human health. There is a risk that the disease agent might be spread to other holdings, to wild birds and from one Member State to other Member States and third countries through the international trade in live birds or their products.
(2) Highly pathogenic avian influenza A virus of subtype H5N1 has been isolated from wild birds in certain parts of the Community and in third countries adjacent to the Community or populated by migratory birds during winter. The likelihood of virus introduction with wild birds is increasing during the forthcoming migratory season.
(3) Where an H5 avian influenza virus collected from poultry is isolated on the territory of a Member State and where, pending the determination of the neuraminidase (N) type or of the pathogenicity index, the clinical picture and the epidemiological circumstances justify the suspicion of highly pathogenic avian influenza caused by highly pathogenic influenza A virus of subtype H5N1 or the presence of highly pathogenic avian influenza, in particular of that subtype, has been confirmed, the affected Member State should apply certain protection measures to minimise the risk of disease spread.
(4) These protective measures should be implemented in addition to those foreseen in the framework of Council Directive 92/40/EEC of 19 May 1992 introducing Community measures for the control of avian influenza(5).
(5) However, the measures provided for in Directive 92/40/EEC are minimum control measures and require supplementary provisions notably on the movement of certain birds and of products from poultry and other birds originating in the zone affected by the disease.
(6) Given the particular disease risk and the epidemiological situation with regard to highly pathogenic avian influenza and taking into account the severe economic impact the disease may have, in particular when occurring in Densely Populated Poultry Areas, supplementary measures should aim at reinforcing the local control measures, regionalising the affected Member State by separating the affected part of the territory from the disease free part thereof, and providing reassurance to the poultry sector and the trade partners about the safety of products dispatched from the disease free part of the country.
(7) Taking account of the differences in disease risk in case of an outbreak of highly pathogenic avian influenza, a high risk area and a low risk area should be established by the affected Member State in close collaboration with the Commission.
(8) If the epidemiological situation so requires, measures appropriate in relation to the areas concerned by the outbreak or suspected outbreak of highly pathogenic avian influenza should be taken, in particular by describing these areas, and keeping this description updated depending on the situation, in Annex I to the present Decision in accordance with the procedure provided for in Article 10(3) or (4) of Directive 90/425/EEC and Article 9(3) or (4) of Directive 89/662/EEC.
(9) In the interests of consistency, it is appropriate to apply for the purposes of this Decision certain definitions provided for in Council Directive 2005/94/EC of 20 December 2005 on Community measures for the control of avian influenza and repealing Directive 92/40/EEC(6), Council Directive 90/539/EEC of 15 October 1990 on animal health conditions governing intra-Community trade in, and imports from third countries of, poultry and hatching eggs(7), Regulation (EC) No 853/2004 of the European Parliament and of the Council of 29 April 2004 laying down specific hygiene rules for food of animal origin(8), Regulation (EC) No 998/2003 of the European Parliament and of the Council of 26 May 2003 on the animal health requirements applicable to the non-commercial movement of pet animals and amending Council Directive 92/65/EEC(9).
(10) The measures laid down in Commission Decision 2005/734/EC of 19 October 2005 laying down biosecurity measures to reduce the risk of transmission of highly pathogenic avian influenza caused by Influenza virus A subtype H5N1 from birds living in the wild to poultry and other captive birds and providing for an early detection system in areas at particular risk(10)should be implemented in the areas affected by the disease.
(11) Council Directive 92/65/EEC of 13 July 1992 laying down animal health requirements governing trade in and imports into the Community of animals, semen, ova and embryos not subject to animal health requirements laid down in specific Community rules referred to in Annex A (I) to Directive 90/425/EEC(11)provides for approved bodies, institutes and centres and a model certificate to accompany animals or their gametes between such approved premises in different Member States. A derogation from the transport restrictions should be envisaged for birds coming from and proceeding to bodies, institutes and centres approved in accordance with that Directive.
(12) Transport of hatching eggs from the protection zones should be permitted under certain conditions. The dispatch of hatching eggs to other countries may be permitted subject in particular to compliance with the conditions referred to in Directive 2005/94/EC. In such cases the animal health certificates provided for in accordance with Directive 90/539/EEC should include a reference to this Decision.
(13) The dispatch from protection zones of meat, minced meat, meat preparations and meat products should be permitted subject to certain conditions, in particular as regards compliance with certain requirements of Regulation (EC) No 853/2004 and of Regulation (EC) No 854/2004 of the European Parliament and of the Council of 29 April 2004 laying down specific rules for the organisation of official controls on products of animal origin intended for human consumption(12).
(14) Council Directive 2002/99/EC of 16 December 2002 laying down the animal health rules governing the production, processing, distribution and introduction of products of animal origin for human consumption(13)establishes a list of treatments rendering meat from restricted areas safe, provides for the possibility to establish a specific identification mark and sets up the identification mark required for meat not authorised for placing on the market for animal health reasons. It is appropriate to permit the dispatch from the protection zones of meat bearing the health mark provided for in that Directive and meat products subjected to treatment referred to therein.
(15) Regulation (EC) No 1774/2002 of the European Parliament and of the Council of 3 October 2002 laying down health rules concerning animal by-products not intended for human consumption(14)authorises the placing on the market of a range of animal by-products, such as gelatine for technical use, materials for pharmaceutical use and others, originating in areas of the Community under animal health restrictions, because those products are considered safe due to the specific conditions of production, processing and utilisation that effectively inactivate possible pathogens or prevent contact with susceptible animals.
(16) This Decision should be reviewed in the light of the transposition of Directive 2005/94/EC by Member States.
(17) Given the disease risk, protection measures should be adopted at Community level in order to address the particular risks in different areas.
(18) The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health,
HAS ADOPTED THIS DECISION:

Subject matter, scope and definitions

1. This Decision lays down certain protection measures to be applied in cases of highly pathogenic avian influenza in poultry in the territory of a Member State (hereinafter the ‘affected Member State’), caused by influenza A virus of subtype H5 suspected (‘suspected outbreak’) or confirmed (‘outbreak’) to be of the neuraminidase type N1, in order to prevent the spread of avian influenza into the disease free parts of the Community through movement of poultry, other birds as well as products thereof.
2. Except as otherwise provided, the definitions of Directive 2005/94/EC shall apply. In addition, the following definitions shall apply:
(a)
‘hatching eggs’ means eggs as defined in Article 2(2) of Directive 90/539/EEC;
(b)
‘wild feathered game’ means game as defined in point 1.5, second indent, and point 1.7 of Annex I to Regulation (EC) No 853/2004;
(c)
‘other captive birds’ means birds as defined in point 6 of Article 2 of Directive 2005/94/EC, including:
(i)
pet animals of the bird species as referred to in Article 3(a) of Regulation (EC) No 998/2003, and
(ii)
birds destined for approved bodies, institutes or centres as defined in Article 2(1) (c) of Directive 92/65/EEC.
3. For the purpose of this Decision the following shall also apply:
(a)
The area listed in Part A of Annex I, hereinafter ‘area A’, shall be considered the area at higher risk including, but not limited to, the protection zone established in accordance with paragraphs 2 and 3 of Article 9 and the surveillance zones established in accordance paragraph 4 of Article 9 of Directive 92/40/EEC.
(b)
The area listed in Part B of Annex I, hereinafter ‘area B’, shall separate area A from the disease free part of the affected Member State, if such part is identified, and the risk of disease in this area shall be considered minimal.
4. The measures set down in this Decision shall be applied without prejudice to the measures to be applied in the event of an outbreak of avian influenza in poultry taken in accordance with Directive 92/40/EEC.

Establishment of areas A and B

1. Immediately following an outbreak or suspected outbreak of highly pathogenic avian influenza caused by influenza A virus of subtype H5 suspected or confirmed to be of the neuraminidase type N1, the affected Member State shall establish areas A and B, having regard to the geographical, administrative, ecological and epizootiological factors relating to avian influenza, and notify them to the Commission, to the other Member States and, as appropriate, to the public.
2. The Commission, in collaboration with the affected Member State, shall examine the areas established by the affected Member State and take the appropriate measures in relation to those areas pursuant to Article 9(3) and (4) of Directive 89/662/EEC or to Article 10(3) or (4) of Directive 90/425/EEC.
3. If the neuraminidase type is confirmed as being different from N1, or the virus as of low pathogenicity, the affected Member State shall abolish the measures taken by it in relation to the areas concerned and notify the Commission and the other Member States.
The Commission, in collaboration with the affected Member State, shall take the appropriate measures pursuant to Article 9(3) or (4) of Directive 89/662/EEC and to Article 10(3) or (4) of Directive 90/425/EEC.
4. If the presence of a highly pathogenic influenza A virus, notably of the subtype H5N1, is confirmed in poultry, the affected Member States shall:
(a)
notify the Commission and the other Member States,
(b)
apply the measures provided for in Article 3(1) and (2) for as long as is necessary having regard to the geographical, administrative, ecological and epizootiological factors relating to avian influenza until the date indicated in Annex I and in any case for at least 21 days in the case of the protection zone and 30 days in the case of the surveillance zone after the date of completion of the preliminary cleansing and disinfection on the outbreak holding in accordance with Article 11 of Directive 92/40/EEC,
(c)
keep the Commission and the other Member States informed about any development with regard to those areas.
The Commission, in collaboration with the affected Member State, shall take the appropriate measures pursuant to Article 9(3) or (4) of Directive 89/662/EEC and to Article 10(3) or (4) of Directive 90/425/EEC.

General prohibition

1. The affected Member State shall ensure that no live poultry and live birds other than poultry, and hatching eggs thereof are:
(a)
dispatched from areas A and B to other Member States and to third countries;
(b)
dispatched from areas A and B to the remaining part of the national territory of the affected Member State;
(c)
transported within areas A and B; and
(d)
moved between areas A and B.
2. The affected Member State shall ensure that no products other than hatching eggs of the species referred to in paragraph 1 and of wild feathered game are:
(a)
dispatched from areas A and B to other Member States and to third countries;
(b)
dispatched from areas A and B to the remaining part of the national territory of the affected Member State; and
(c)
transported between areas A and B.

Derogations for live birds and day-old chicks

1. By way of derogation from Article 3(1), the affected Member State may authorise the transport of poultry or farmed feathered game, including spent laying hens,
(a)
from holdings in the protection zone for immediate slaughter to a slaughterhouse preferably located in the protection zone, if that is not possible, to a slaughterhouse outside the protection zone in the affected Member State which is designated by the competent authority;
(b)
from holdings in the surveillance zone, during the 15 days following the establishment of the zone, directly to a slaughterhouse within or outside the surveillance zone in the affected Member State which is designated by the competent authority;
(c)
from holdings in area A situated either within the surveillance zone after 15 days following its establishment or outside the surveillance zone, or in area B, to slaughterhouses in the affected Member State designated by the competent authority;
(d)
from holdings situated outside the area A or area B for immediate slaughter in a slaughterhouse designated by the competent authority and situated in area A or area B;
(e)
from holdings situated outside the area A or area B in transit by major highways or railways through area A outside the protection zone or area B.
2. By way of derogation from Article 3(1), the affected Member State may authorise the transport of day-old chicks:
(a)
from a hatchery situated in the protection zone to a holding within the protection or surveillance zone at which there are no other poultry and which is placed under the official control provided for in Article 8(2) of Directive 92/40/EEC;
(b)
from a hatchery situated in the surveillance zone to a holding or shed of such holding in the same Member State provided that appropriate biosecurity measures are applied and the holding is placed under official surveillance following the transport and day-old chicks shall remain on the holding of destination for at least 21 days;
(c)
from a hatchery situated in area A in the surveillance zone to any holding provided, they are hatched from eggs collected from holdings situated outside the protection and surveillance zone, and that the hatchery can ensure by its logistics and biosecurity working conditions that no contact has occurred between these eggs and any other hatching eggs or day-old-chicks originating from poultry flocks within those zones and which are therefore of a different health status;
(d)
from a hatchery situated in the part of area A outside the surveillance zone or in area B, and at least 10 km away from any suspected or infected hatchery or holding, to holdings under official control in the affected Member State;
(e)
from a hatchery situated in the part of area A outside the protection zone or in area B to holdings within or outside the area A, provided that the day-old chicks are hatched from eggs complying with the requirements in Article 5(1)(d).
3. By way of derogation from Article 3(1), the affected Member State may authorise the transport of ready-to-lay pullets, turkeys for fattening and other poultry or farmed feathered game:
(a)
from holdings in the protection zone to a holding within the surveillance zone at which there are no other poultry and which is placed under the official control provided for in Article 8(2) of Directive 92/40/EEC;
(b)
from holdings in the surveillance zone after the 15 days following its establishment to a holding in which there is no other poultry in the same Member State; that holding shall be placed under official surveillance following the arrival of the ready-to-lay poultry and the ready-to-lay poultry shall remain on the holding of destination for at least 21 days;
(c)
from holdings situated in the part of area A outside the surveillance zone or area B, and at least 10 km away from any suspected holding, to holdings under official control in the affected Member State.
4. By way of derogation from Article 3(1), the affected Member State may authorise transport of birds accompanying their owner to premises outside the area A or area B, if the consignment either consists of not more than 5 caged birds from holdings not keeping poultry or is destined for a quarantine established in accordance with Decision 2000/666/EC, and the birds are accompanied by a veterinary certificate in accordance with the model set up in Annex II, certifying compliance with the established animal health conditions, where required based on owners’ declaration in accordance with the model set up in Annex III.
5. The animal health certificates in accordance with Model 2 of Annex IV to Council Directive 90/539/EEC accompanying consignments of day-old chicks referred to in paragraph 2(c) and (e) shall include the words:
‘The consignment complies with the animal health conditions laid down in Commission Decision 2006/135/EC.’
6. Movements allowed in paragraphs 1(a), 2(a) and 3(a) shall be directly executed, under official control. They shall be authorised only after the official veterinarian has carried out a health inspection of the holding. The means of transport used must be cleaned and disinfected before and after use.

Derogations for hatching eggs

1. By way of derogation from Article 3(1), the affected Member State may authorise the dispatch of hatching eggs:
(a)
collected on holdings situated on the day of collection in the protection zone to a hatchery designated by the competent authority; provided the eggs and their packing are disinfected before dispatch;
(b)
collected in holdings situated on the day of collection in the surveillance zone to a hatchery in the affected Member State which is designated by the competent authority, provided the eggs and their packaging are disinfected before dispatch;
(c)
collected in holdings situated on the day of collection in area A outside the surveillance zone or area B, and at least 10 km away from any suspect holding, to a designated hatchery in the affected Member State, or following agreement between the competent authorities, to a designated hatchery in another Member State or third country;
(d)
collected from holdings in area A outside the protection or surveillance zone or in area B on which the poultry has tested negative in a serological survey for avian influenza capable of detecting 5 % prevalence of disease with at least a 95 % level of confidence and traceability is ensured, to hatcheries within or outside the areas A or B.
2. Movements allowed in paragraph 1(a) shall be directly executed, under official control and only after the official veterinarian has carried out a health inspection of the holding and the means of transport are cleaned and disinfected before and after use.
3. The animal health certificates in accordance with Model 1 of Annex IV to Council Directive 90/539/EEC accompanying consignments of hatching eggs referred to in paragraph 1(c) and (d) to other Member States shall include the words:
‘The consignment complies with the animal health conditions laid down in Commission Decision 2006/135/EC.’

Derogations for meat, minced meat, meat preparations, mechanically separated meat and meat products

1. By way of derogation from Article 3(2), the affected Member State shall authorise the dispatch of:
(a)
fresh meat from poultry, including meat from ratites, referred to in Article 4(1) (a) and (b) if such meat is marked with the identification mark provided for in Annex II to Directive 2002/99/EC and is intended for transport to an establishment for treatment as required for avian influenza in table 1(a), (b) or (c) of Annex III to that Directive;
(b)
fresh meat from poultry, including meat from ratites, originating in area A, outside the protection zone and the surveillance zones during 15 days following its establishment, or area B, or produced from poultry referred to in Article 4(1)(d) and produced in accordance with Annex II and Sections II and III of Annex III to Regulation (EC) No 853/2004 and controlled in accordance with Sections I, II, III, and Chapters V and VII of Section IV of Annex I to Regulation (EC) No 854/2004;
(c)
minced meat, meat preparations, mechanically separated meat and meat products containing meat referred to in point (b) and produced in accordance with Sections V and VI of Annex III to Regulation (EC) No 853/2004;
(d)
fresh meat from poultry and farmed feathered game, minced meat and meat preparations and mechanically separated meat containing such meat, obtained from slaughter poultry or farmed feathered game originating in the part of area A outside the protection zone from area A or area B into the remaining part of its national territory of, if such meat:
(i)
was identified with a round stamp as setup in accordance with Article 4(2) of Directive 2002/99/EC in Annex IV to the present Decision; and
(ii)
was obtained, cut, stored and transported separately from other fresh meat from poultry or farmed feathered game destined for dispatch to other Member States or for exports to third countries; and
(iii)
is used in such a way as to avoid it being introduced into meat products or meat preparations intended for placing on the market in other Member States or for export to third countries, unless it has undergone the treatment as required for avian influenza specified in table 1(a), (b) or (c) of Annex III to Directive 2002/99/EC.
2. By way of derogation from Article 3(2), the affected Member State shall authorise the dispatch of:
(a)
fresh meat from wild feathered game originating in area A or area B, if such meat is marked with the health mark provided for in Annex II to Directive 2002/99/EC and is intended for transport to an establishment for treatment as required for avian influenza in table 1(a), (b) or (c) of Annex III to that Directive;
(b)
meat products produced from meat from wild feathered game originating in area A or in area B which were subjected to a treatment as required for avian influenza in table 1(a), (b) or (c) of Annex III to Directive 2002/99/EC;
(c)
fresh meat from wild feathered game originating outside the areas A and B and produced in establishments within area A or area B in accordance with Section IV of Annex III to Regulation (EC) No 853/2004 and controlled in accordance with Chapter VIII of Section IV of Annex I to Regulation (EC) No 854/2004;
(d)
minced meat, meat preparations, mechanically separated meat and meat products containing meat referred to in point (c) and produced in establishments situated in area A or area B in accordance with Sections V and VI of Annex III to Regulation (EC) No 853/2004.
3. The affected Member State shall ensure that the products referred to in paragraphs 1(b), (c) and 2(b), (c), (d) are accompanied by commercial documents stating:
‘The consignment complies with the animal health conditions laid down in Commission Decision 2006/135/EC.’

Derogations for eggs for human consumption and egg products

1. By way of derogation from Article 3(2), the affected Member State may authorise the dispatch of eggs collected from holdings in the protection or surveillance zone:
(a)
for human consumption to a packing centre designated by the competent authority, provided that they are packed in disposable packaging and that all biosecurity measures required by the competent authority are applied;
(b)
to an establishment for the manufacture of egg products as set out in Chapter II of Section X of Annex III to Regulation (EC) No 853/2004 to be handled and treated in accordance with Chapter XI of Annex II to Regulation (EC) No 852/2004;
(c)
for disposal in accordance with Regulation (EC) No 1774/2002.
2. By way of derogation from Article 3(2), the dispatch to any destination shall be allowed for:
(a)
eggs for human consumption collected from holdings in area A, outside the protection or surveillance zone, or area B;
(b)
pasteurised egg products in accordance with Chapter II of Section X of Annex III to Regulation (EC) No 853/2004.
3. The affected Member State shall ensure that consignments of eggs for human consumption referred to in paragraph 1(a) are accompanied by commercial documents stating:
‘The consignment complies with the animal health conditions laid down in Commission Decision 2006/135/EC.’

Derogation for animal by-products

1. By way of derogation from Article 3(2), the affected Member State shall authorise:
(a)
the dispatch from area A or area B of the animal by products complying with the conditions set up in Chapters II (A), III (B), IV (A), VI (A and B), VII (A), VIII (A), IX (A)and X (A) of Annex VII, and Chapters II (B), III (II) (A) and VII (A) (1)(a) of Annex VIII to Regulation (EC) No 1774/2002;
(b)
the dispatch from area B of untreated feathers or parts of feathers in accordance with Chapter VIII (A) (1) (a) of Annex VIII to Regulation (EC) No 1774/2002, produced from poultry or farmed feathered game;
(c)
the dispatch from area A or area B of feathers and parts of feathers that have been treated with a steam current, or by some other method that ensures that no pathogens remains, produced from poultry or farmed feathered game.
2. The affected Member State shall ensure that the products referred to in paragraph 1(b) and (c) of this Article are accompanied by a commercial document in accordance with Chapter X of Annex II to Regulation (EC) No 1774/2002 stating, in the case of the products referred to in paragraph 1(c) of this Article, in point 6.1 of that document that those products have been treated with a steam current or by some other method ensuring that no pathogens remains.
However, that commercial document shall not be required for processed decorative feathers, processed feathers carried by travellers for their private use or consignments of processed feathers sent to private individuals for non-industrial purpose.

Conditions for movements

1. Where movements of animals or products thereof covered by this Decision are authorised under Articles 4, 5, 6, 7 and 8, the authorisation shall be based on the favourable outcome of a risk assessment carried out by the competent authority and all appropriate biosecurity measures shall be taken to avoid the spread of avian influenza.
2. Where the dispatch, movement or transport of products referred to in paragraph 1 are authorised under Articles 5, 6, 7 and 8, subject to justified conditions or limitations, they must be obtained, handled, treated, stored and transported without compromising the animal health status of other products fulfilling all the animal health requirements for trade, placing on the market or export to third countries.

Compliance and Information

All Member States shall immediately adopt and publish the measures necessary to comply with this Decision. They shall immediately inform the Commission thereof.
The affected Member State shall apply those measures as soon as it reasonably suspects the presence of highly pathogenic avian influenza virus, in particular of the subtype H5N1, in poultry.
The affected Member State shall regularly provide to the Commission and the other Member States the necessary information on the epidemiology of the disease and, where appropriate the additional control and surveillance measures and the awareness campaigns implemented.

Addressee

This Decision is addressed to the Member States.

PART A

ANNEX IArea A as referred to in Article 2(1):

ISO Country Code | Member State | Area A | Date until applicable
| | |
| | | PART BArea B as referred to in Article 2(2):

ISO Country Code | Member State | Area B | Date until applicable
| | |
| | |

ANNEX IIModel certificate for the movement of pet birds in accordance with Article 4(4):

EUROPEAN COMMUNITY Intra trade certificate
I.1. Consignor
Name Address Postal code
I.2. Certificate reference number
I.2.a. Local reference number:
I.3. Central Competent Authority
I.4. Local Competent Authority
I.5. Consignee Name Address Postal code
I.6. No.(s) of accompanying documents
I.7. I.8. Country of origin
ISO code
I.9. Region of origin
Code
I.10. Country of destination
ISO code
I.11. Region of destination
Code
I.12. Place of origin Holding Approved body Other
Name Approval number
Address Postal code
I.13. Place of destination Holding Approved body Quarantine
Other
Name Approval number
Address Postal code
I.14. Place of loading Postal code
I.15. Date and time of departure
I.16. Means of transport Aeroplane Ship Railway wagon
Road vehicle Other
Identification:
I.17. Transporter Name Approval number
Address Postal code Member state
I.18. Animal species/Product
I.19. Commodity code (CN code)
I.20. Number/Quantity
I.21. I.22. Number of packages
I.23. Identification of container/Seal number
I.24. I.25. Animals certified as/products certified for:
Breeding Pets Approved body Quarantine
I.26. Transit through third country
Third country ISO code
Exit point Code
Entry point BIP unit no.:
I.27. Transit through Member states
Member state ISO code
Member state ISO code
Member state ISO code
I.28. I.29. I.30. I.31. Identification of the animals/products Species (Scientific name) Identification system Identification number Age Sex Quantity
Part I: Details of consignment presented

MEMBER STATE Pet birds
II. Health information
II.a. Certificate reference number
II.b. Local reference number
I, the undersigned official veterinarian of (insert name of country) certify that: 1. The birds described in point I.31.have been subjected today, within 48 hour or the last working day prior to dispatch, to a clinical inspection and found free of obvious signs of disease; 2. The birds comply with at least one of the following conditions:
either [they have been confined on the premises specified in point I.12 under official supervision for at least 30 days prior to dispatch and effectively protected from contacts with other birds] (1) or [they are destined, as indicated in point I.13. for a quarantine station approved in accordance with Article 3(4) of Decision 2000/666/EC] (1) 3. The owner or the representative of the owner has declared:
3.1. The birds will be accompanied during the movement by a person that is responsible for the animals.
3.2. The animals are not intended for commercial purposes.
3.3. During the period between the pre-movement veterinary inspection and the factual departure the birds will remain isolated from any possible contact with other birds.
either [3.4. The animals have undergone the 30 days pre-movement isolation without coming into contact to any other birds not covered by this certificate.] (1) or [3.4. I have made arrangements for the 30 days post-introduction quarantine at the quarantine premises of …, as indicated in point I.13. of the certificate.] (1) Notes
(1) Delete as necessary.
(2) The certificate is valid for 10 days. In case of transport by boat the validity is prolonged by the time of the sea voyage.
Official veterinarian:
Name (in capital letters): Qualification and title:
Date: Signature:
Stamp:
Part II: Certification

ANNEX IIIDeclaration of the owner or representative of the owner of the pet birds as required by Article 4 (4):

I, the undersigned owner (a)/representative of the owner (a) declare that: 1. The birds will be accompanied during the movement by a person that is responsible for the animals. 2. The animals are not intended for commercial purposes. 3. During the period between the pre-movement veterinary inspection and the factual departure the birds will remain isolated from any possible contact with other birds. 4. The animals have undergone the 30 days pre-movement isolation without coming into contact to any other birds not covered by this certificate (a). 5. I have made arrangements for the 30 days post-introduction quarantine at the quarantine premises of , as indicated in point I.13. of the certificate (a).
Date and Place
Signature
(a) delete as appropriate

ANNEX IVDetails of the identification mark referred to in Article 6 (1) (d) (i):

Dimensions:XYZ(1)= 8 mm1234(2)= 11 mmCircle outer diameter= not less than 30 mmLine thickness of circle= 3 mm | | Dimensions:XYZ(1)= 8 mm1234(2)= 11 mmCircle outer diameter= not less than 30 mmLine thickness of circle= 3 mm |
| Dimensions:XYZ(1)= 8 mm1234(2)= 11 mmCircle outer diameter= not less than 30 mmLine thickness of circle= 3 mm
(1) means the relevant country code provided for in point 6 of Part B of Section I of Annex II to Regulation (EC) No 853/2004.
(2) means the approval number of the establishment referred to in point 7 of Part B of Section I of Annex II to Regulation (EC) No 853/2004.

Pending: 32006D0109

17.2.2006 EN Official Journal of the European Union L 47/59
(1) The Council, by Regulation (EC) No 1212/2005(2)(the definitive Regulation), imposed definitive anti-dumping duties on imports into the Community of certain castings originating in the People’s Republic of China (PRC).
(2) Upon publication of the definitive Regulation, no undertakings could be accepted by the Commission. During the investigation leading to the imposition of definitive measures several exporting producers had indicated their intention to offer a price undertaking but they had failed to submit sufficiently substantiated undertaking offers within the deadlines set in Article 8(2) of the basic Regulation. Nevertheless, as set out in recital 152 of the definitive Regulation, the Council, in view of the complexity of the issue for the economic operators in question (predominantly small and medium-sized enterprises) and given that the definitive disclosure was not preceded by a provisional disclosure, considered that they should exceptionally be allowed to complete their undertaking offers beyond the said deadline.
(3) Subsequent to the abovementioned deadline, the China Chamber of Commerce for Import and Export of Machinery and Electronics Products (CCCME) together with 20 cooperating Chinese companies or cooperating groups of companies, including the related importer of one of the groups (the companies) offered a joint undertaking. The undertaking stipulates that a breach by any of the companies or the CCCME shall be considered as a breach of the undertaking by all signatories. However, given that the resales of the related importer in the Community are not under the aegis of the CCCME, any violation by that related importer or its related exporters in the PRC shall be considered as a breach only from that particular group. The undertaking offer was supported by the Chinese authorities.
(4) According to this undertaking, the CCCME and the companies undertake to ensure that the product concerned is exported at or above a minimum price set at a level that eliminates the injurious effects of dumping. In addition, the offer made foresees the indexation of the minimum price of the product concerned in accordance with public international quotations for its main raw material, i.e. pig iron, given that the casting prices vary significantly depending on the prices of pig iron.
(5) In view of the foregoing, the Commission considers that the joint undertaking offered by the CCCME and the companies can be accepted since it eliminates the injurious effects of dumping. Moreover, the regular and detailed reports which the CCCME and the companies undertook to provide to the Commission will allow effective monitoring, and it is considered that the risk of circumvention of the undertaking is limited.
(6) In order to enable the Commission to monitor effectively the compliance with the undertaking, when the request for release for free circulation pursuant to the undertaking is presented to the relevant customs authority, exemption from the duty will be conditional upon the presentation of an invoice containing at least the items of information listed in the Annex to Council Regulation (EC) 268/2006(3). This level of information is also necessary to enable customs authorities to ascertain with sufficient precision that the shipment corresponds to the commercial documents. Where no such invoice is presented, or when it does not correspond to the product presented to customs, the appropriate rate of anti-dumping duty established in the above-mentioned Regulation will instead be payable.
(7) To further ensure the effective respect of the undertaking, the importers have been made aware by the above Council Regulation that any violation of the undertaking may lead to the retrospective application of the anti-dumping duty for the relevant transaction.
(8) In the event of a breach or withdrawal of the undertaking, or in case of a withdrawal of acceptance of the undertaking by the Commission, the anti-dumping duty imposed in accordance with Article 9(4) of the basic Regulation shall automatically apply pursuant to Article 8(9) of the basic Regulation,
Company Taric additional code
Beijing Tongzhou Dadusche Foundry Factory, East of Dongtianyang Village, Dadushe, Tongzhou Beijing A708
Botou City Simencun Town Bai Fo Tang Casting Factory, Bai Fo Tang Village, Si Men Cun Town, Bo Tou City, 062159, Hebei Province A681
Botou City Wangwu Town Tianlong Casting Factory, Changle Village, Wangwu Town, Botou City, Hebei Province A709
Changan Cast Limited Company of Yixian Hebei, Taiyuan main street, Yi County, Hebei Province, 074200 A683
Changsha Jinlong Foundry Industry Co., Ltd, 260 Jinchang Road, JinJing Town, Changsha, Hunan A710
Changsha Lianhu Foundry, Lianhu Village, Yuhuating Town, Yuhua District, Changsha, Hunan A711
Manufactured and sold by GB Metal Products Co., Ltd, Zhuanlu Town, Dingzhou, Hebei or manufactured by GB Metal Products Co., Ltd, Zhuanlu Town, Dingzhou, Hebei and sold by its related sales company GB International Trading Shanghai Co., Ltd, B301-310 Yinhai Building, 250 Cao Xi Road, Shanghai A712
Guiyang Bada Foundry Co., Ltd, Mengguan Huaxi Guiyang, Guizhou A713
Hebei Jize Xian Ma Gang Cast Factory, Nankai District. Xiao Zhai Town, Jize County, Handan City, Hebei A714
Manufactured and sold by Hebei Shunda Foundry Co., Ltd, Qufu Road, Quyang, 073100, PRC or manufactured by Hebei Shunda Foundry Co., Ltd, Qufu Road, Quyang, 073100, PRC and sold by its related sales company Success Cast Tech-Ltd, 603A Huimei Business Centre 83 Guangzhou Dadao(s), Guangzhou 510300 A715
Hong Guang Handan Cast Foundry Co., Ltd, Nankai District, Xiao Zhai Town, Handou City, Jize County, Hebei A716
Manufactured by (i) Zibo Benito Metalwork Co., Ltd, No 1, Shitanwu, Boyi Road, Boshan District, Zibo City, Shandong, 255201, (ii) Benito (Tianjin) Metals Products Co., Ltd, Da Lu Zhuang Village, Bei Zha Kou Town, Jin Nan District, Tianjin or (iii) Qingdao Benito Metals Products Co. Ltd, Yan Jia Ling Village, Tong Ji Jie Dao Office, Jimo City, Qingdao, Shandong Province and exclusively imported by Fundició Dúctil Benito, Via Ausetania, 11, E-08560 Manlleu, Barcelona, Spain A717
Qingdao Qitao Casting Co., Ltd, Nan Wang Jia Zhuang Village, Da Xin Town, Jimo City, Qingdao, Shandong Province, 266200 A718
Shandong Huijin Stock Co., Ltd, North of Kouzhen Town, Laiwu City, Shandong Province, 271114 A684
Shane City Fangyuan Casting Co., Ltd, West of Nango Village, Shiliting Town, Shane City, Hebei Province A719
Shanxi Yuansheng Casting and Forging Industrial Co., Ltd, No 8 DiZangAn, Taiyuan, Shanxi, 030002 A680
Tianjin Fu Xing Da Casting Co., Ltd, West of Nan Yang Cun Village, Jin Nan District, 300350, Tianjin A720
Weifang Jianhua Casting Co., Ltd, Kai Yuan Jie Dao Office, Hanting District, Weifang City, Shandong Province A721
Zibo City Boshan Guangyuan Casting Machinery Factory, Xiangyang Village, Badou Town, Boshan District, Zibo City Shandong Province A722
Zibo Dehua Machinery Co., Ltd, North of Lanyan Street, Zibo High-tech Developing Zone A723
THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Council Regulation (EC) No 384/96 of 22 December 1995 on protection against dumped imports from countries not members of the European Community(1)(the basic Regulation), and in particular Article 8 thereof,
After consulting the Advisory Committee,
HAS DECIDED AS FOLLOWS:

Article 1
The undertaking offered by China Chamber of Commerce for Import and Export of Machinery and Electronics Products (CCCME) and the cooperating producers mentioned in the table, in connection with the anti-dumping proceeding concerning imports of certain castings originating in the People’s Republic of China is hereby accepted.

Article 2
This Decision shall enter into force on the day following its publication in theOfficial Journal of the European Union.

THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Council Regulation (EC) No 384/96 of 22 December 1995 on protection against dumped imports from countries not members of the European Community(1)(the basic Regulation), and in particular Article 8 thereof,
After consulting the Advisory Committee,
HAS DECIDED AS FOLLOWS:
The undertaking offered by China Chamber of Commerce for Import and Export of Machinery and Electronics Products (CCCME) and the cooperating producers mentioned in the table, in connection with the anti-dumping proceeding concerning imports of certain castings originating in the People’s Republic of China is hereby accepted.
This Decision shall enter into force on the day following its publication in theOfficial Journal of the European Union.

Pending: 32005D0648

15.9.2005 EN Official Journal of the European Union L 238/16
(1) On 23 August 2005 Bulgaria confirmed an outbreak of Newcastle disease in the administrative district of Vratsa in Bulgaria. Newcastle disease is a highly contagious viral disease in poultry and birds and there is a risk that the disease agent might be introduced via international trade in live poultry and poultry products.
(2) In view of the animal health risk of disease introduction into the Community, it is therefore appropriate to take measures in relation to imports of live poultry, ratites, farmed and wild feathered game birds and hatching eggs of these species from Bulgaria.
(3) Bulgaria has communicated further information on the disease situation and asked for regionalisation to suspend importation into the Community from the administrative district of Vratsa only, since the situation in the rest of the country appears to be satisfactory. The information available at present gives the possibility to reduce the protection measures to a specific region.
(4) Therefore, the importation into the Community from the administrative district of Vratsa in Bulgaria should be suspended for fresh meat of poultry, ratites and wild and farmed feathered game, meat preparations and meat products consisting of, or containing meat of those species, obtained from birds slaughtered after 16 July 2005.
(5) Commission Decision 2005/432/EC(3)lays down the list of third countries from which Member States may authorise the importation of meat products, and establishes treatment regimes in order to prevent the risk of disease transmission via such products. The treatment that must be applied to the product depends on the health status of the country of origin, in relation to the species the meat is obtained from; in order to avoid an unnecessary burden on trade, imports of poultry meat products originating in Bulgaria treated to a temperature of at least 70 °C throughout the product should continue to be authorised.
(6) The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health,
(a) fresh meat of poultry, ratites, farmed and wild feathered game; and
(b) meat preparations and meat products consisting of, or containing meat of, the species referred to in point (a).
THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Council Directive 91/496/EEC of 15 July 1991 laying down the principles governing the organisation of veterinary checks on animals entering the Community from third countries and amending Directives 89/662/EEC, 90/425/EEC and 90/675/EEC(1), and in particular Article 18 thereof,
Having regard to Council Directive 97/78/EC of 18 December 1997 laying down the principles governing the organisation of veterinary checks on products entering the Community from third countries(2), and in particular Article 22 thereof,
(1) On 23 August 2005 Bulgaria confirmed an outbreak of Newcastle disease in the administrative district of Vratsa in Bulgaria. Newcastle disease is a highly contagious viral disease in poultry and birds and there is a risk that the disease agent might be introduced via international trade in live poultry and poultry products.
(2) In view of the animal health risk of disease introduction into the Community, it is therefore appropriate to take measures in relation to imports of live poultry, ratites, farmed and wild feathered game birds and hatching eggs of these species from Bulgaria.
(3) Bulgaria has communicated further information on the disease situation and asked for regionalisation to suspend importation into the Community from the administrative district of Vratsa only, since the situation in the rest of the country appears to be satisfactory. The information available at present gives the possibility to reduce the protection measures to a specific region.
(4) Therefore, the importation into the Community from the administrative district of Vratsa in Bulgaria should be suspended for fresh meat of poultry, ratites and wild and farmed feathered game, meat preparations and meat products consisting of, or containing meat of those species, obtained from birds slaughtered after 16 July 2005.
(5) Commission Decision 2005/432/EC(3)lays down the list of third countries from which Member States may authorise the importation of meat products, and establishes treatment regimes in order to prevent the risk of disease transmission via such products. The treatment that must be applied to the product depends on the health status of the country of origin, in relation to the species the meat is obtained from; in order to avoid an unnecessary burden on trade, imports of poultry meat products originating in Bulgaria treated to a temperature of at least 70 °C throughout the product should continue to be authorised.
(6) The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health,
HAS ADOPTED THIS DECISION:

Article 1
Member States shall suspend imports from the administrative districts in Bulgaria listed in the Annex to this Decision of live poultry, ratites, farmed and wild feathered game and hatching eggs of these species.

Article 2
Member States shall suspend imports from the administrative districts in Bulgaria listed in the Annex to this Decision of:
(a)
fresh meat of poultry, ratites, farmed and wild feathered game; and
(b)
meat preparations and meat products consisting of, or containing meat of, the species referred to in point (a).

Article 3
1. By way of derogation from Article 2(a) and (b), Member States shall authorise imports of the products covered by that Article which have been obtained from poultry, ratites, farmed and wild feathered game coming from the administrative districts in Bulgaria listed in the Annex to this Decision and which were slaughtered or killed before 16 July 2005.
2. In the veterinary certificates accompanying consignments of the products referred to in paragraph 1, the following words shall be included:
‘Fresh poultry meat/fresh ratite meat/fresh meat of wild feathered game/fresh meat of farmed feathered game/meat product consisting of, or containing meat of poultry, ratites, farmed or wild feathered game meat/meat preparation consisting of, or containing meat of poultry, ratites, farmed or wild feathered game meat(*1)in accordance with Article 3(1) of Decision 2005/648/EC.
3. By way of derogation from Article 2(b) of this Decision, Member States shall authorise imports of meat products consisting of, or containing meat of, poultry, ratites, farmed and wild feathered game, when the meat of these species has undergone one of the specific treatments referred to in points B, C or D in Part 4 of Annex II to Decision 2005/432/EC.

Article 4
The Member States shall amend the measures they apply to trade so as to bring them into compliance with this Decision and they shall give immediate appropriate publicity to the measures adopted. They shall immediately inform the Commission thereof.

Article 5
This Decision shall apply until 23 August 2006.

Article 6
This Decision is addressed to the Member States.

THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Council Directive 91/496/EEC of 15 July 1991 laying down the principles governing the organisation of veterinary checks on animals entering the Community from third countries and amending Directives 89/662/EEC, 90/425/EEC and 90/675/EEC(1), and in particular Article 18 thereof,
Having regard to Council Directive 97/78/EC of 18 December 1997 laying down the principles governing the organisation of veterinary checks on products entering the Community from third countries(2), and in particular Article 22 thereof,
(1) On 23 August 2005 Bulgaria confirmed an outbreak of Newcastle disease in the administrative district of Vratsa in Bulgaria. Newcastle disease is a highly contagious viral disease in poultry and birds and there is a risk that the disease agent might be introduced via international trade in live poultry and poultry products.
(2) In view of the animal health risk of disease introduction into the Community, it is therefore appropriate to take measures in relation to imports of live poultry, ratites, farmed and wild feathered game birds and hatching eggs of these species from Bulgaria.
(3) Bulgaria has communicated further information on the disease situation and asked for regionalisation to suspend importation into the Community from the administrative district of Vratsa only, since the situation in the rest of the country appears to be satisfactory. The information available at present gives the possibility to reduce the protection measures to a specific region.
(4) Therefore, the importation into the Community from the administrative district of Vratsa in Bulgaria should be suspended for fresh meat of poultry, ratites and wild and farmed feathered game, meat preparations and meat products consisting of, or containing meat of those species, obtained from birds slaughtered after 16 July 2005.
(5) Commission Decision 2005/432/EC(3)lays down the list of third countries from which Member States may authorise the importation of meat products, and establishes treatment regimes in order to prevent the risk of disease transmission via such products. The treatment that must be applied to the product depends on the health status of the country of origin, in relation to the species the meat is obtained from; in order to avoid an unnecessary burden on trade, imports of poultry meat products originating in Bulgaria treated to a temperature of at least 70 °C throughout the product should continue to be authorised.
(6) The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health,
HAS ADOPTED THIS DECISION:
Member States shall suspend imports from the administrative districts in Bulgaria listed in the Annex to this Decision of live poultry, ratites, farmed and wild feathered game and hatching eggs of these species.
Member States shall suspend imports from the administrative districts in Bulgaria listed in the Annex to this Decision of:
(a)
fresh meat of poultry, ratites, farmed and wild feathered game; and
(b)
meat preparations and meat products consisting of, or containing meat of, the species referred to in point (a).
1. By way of derogation from Article 2(a) and (b), Member States shall authorise imports of the products covered by that Article which have been obtained from poultry, ratites, farmed and wild feathered game coming from the administrative districts in Bulgaria listed in the Annex to this Decision and which were slaughtered or killed before 16 July 2005.
2. In the veterinary certificates accompanying consignments of the products referred to in paragraph 1, the following words shall be included:
‘Fresh poultry meat/fresh ratite meat/fresh meat of wild feathered game/fresh meat of farmed feathered game/meat product consisting of, or containing meat of poultry, ratites, farmed or wild feathered game meat/meat preparation consisting of, or containing meat of poultry, ratites, farmed or wild feathered game meat(*1)in accordance with Article 3(1) of Decision 2005/648/EC.
3. By way of derogation from Article 2(b) of this Decision, Member States shall authorise imports of meat products consisting of, or containing meat of, poultry, ratites, farmed and wild feathered game, when the meat of these species has undergone one of the specific treatments referred to in points B, C or D in Part 4 of Annex II to Decision 2005/432/EC.
The Member States shall amend the measures they apply to trade so as to bring them into compliance with this Decision and they shall give immediate appropriate publicity to the measures adopted. They shall immediately inform the Commission thereof.
This Decision shall apply until 23 August 2006.
This Decision is addressed to the Member States.
ANNEXAdministrative district of Vratsa

Pending: 32005D0432

14.6.2005 EN Official Journal of the European Union L 151/3
(1) Commission Decision 97/41/EC of 18 December 1996 establishing health conditions and a public health certificate for the importation from third countries of meat products obtained from poultry meat, farmed game meat, wild game meat, and rabbit meat(3)lays down public health conditions for the importation into the Community of certain meat products.
(2) Commission Decision 97/221/EC of 28 February 1997 laying down the animal health conditions and model veterinary certificates in respect of imports of meat products from third countries and revoking Decision 91/449/EEC(4)lays down animal health conditions and certification rules for the importation into the Community of certain meat products.
(3) Commission Decision 97/222/EC of 28 February 1997 laying down the list of third countries from which the Member States authorise the importation of meat products(5)provides for the importation into the Community of certain meat products provided that such products have undergone the appropriate treatment and comply with Community veterinary certification requirements.
(4) Council Directive 72/462/EEC of 12 December 1972 on health and veterinary inspection problems upon importation of bovine, ovine and caprine animals and swine, fresh meat or meat products from third countries(6)lays down animal health requirements for the importation into the Community of certain meat products. Council Directive 2004/68/EC(7)provides for the repeal of Directive 72/462/EEC from 1 January 2006.
(5) Directive 2002/99/EC lays down the animal health rules governing the production, processing, distribution and introduction of products of animal origin for human consumption. That Directive is to be implemented by the Member States before 1 January 2005.
(6) Council Directive 77/99/EEC of 21 December 1976 on health problems affecting the production and marketing of meat products and certain other products of animal origin(8)will be in force till 1 January 2006 when it will be repealed and any definition of meat based products in acts adopted before 1 January 2006 must refer to Directive 77/99/EEC.
(7) In view of the entry into force of Directive 2002/99/EC, it is necessary to amend and update Community public and animal health conditions and certification requirements for the importation into the Community of meat products derived from domestic bovines, porcines, ovines, caprines, equidae, poultry, farmed game, domestic rabbits and wild game.
(8) In addition, in the interests of clarity and consistency of Community legislation, it is appropriate to lay down the public and animal health conditions in a single model health certificate for importation of meat products into the Community.
(9) Due to differences in the animal health situation in third countries, it is appropriate to lay down rules concerning treatments for meat products from third countries or parts of third countries prior to their importation into the Community.
(10) In the interests of clarity and consistency of Community legislation, it is appropriate to repeal Decisions 97/41/EC, 97/221/EC and 97/222/EC and replace them by this Decision. Accordingly, this Decision should contain the animal and public health conditions and certification requirements, together with the list of third countries and the treatments required for the importation of various categories of meat products into the Community.
(11) Health conditions and veterinary certification should apply without prejudice to the requirement of Commission Decision 2004/432/EC of 29 April 2004 on the approval of residue monitoring plans submitted by third countries in accordance with Directive 96/23/EC(9).
(12) Council Directive 97/78/EC of 18 December 1997 laying down the principles governing the organisation of veterinary checks on products entering the Community from third countries(10)lays down rules concerning veterinary checks on animal products introduced into the Community from third countries for the importation and transit of products of animal origin in the Community, including certain certification requirements.
(13) In the interests of animal and public health and in order to prevent the spread of animal diseases in the Community, a new specific model public and animal health certificate should be established in this Decision. In addition, it should be provided that transit through the Community of consignments of meat products is only permitted where those products come from third countries or parts of third countries whose products are not prohibited for introduction into the Community.
(14) It is necessary to lay down specific conditions for transit via the Community of consignments of meat products to and from Russia due to the geographical situation of Kaliningrad and taking into account climatic problems impeding the use of some ports at certain times of the year.
(15) Commission Decision 2001/881/EC of 7 December 2001 drawing up a list of border inspection posts agreed for veterinary checks on animals and animal products from third countries and updating the detailed rules concerning the checks to be carried out by the experts of the Commission(11), specifies the Border Inspection Posts authorised to control the transit of consignments of meat products to and from Russia via the Community
(16) The treatments provided for poultry meat products originating in Bulgaria and Israel and for wild swine meat products originating in Switzerland should be reviewed in order to bring them into line with the current import conditions for fresh meat of the concerned species from those countries.
(17) The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health,
(a) domestic poultry of the following species: domestic fowl, turkeys, guinea fowl, geese and ducks;
(b) domestic animals of the following species: bovine animals, includingBubalus bubalis, Bison bison, swine, sheep, goats and solipeds;
(c) farmed game and domestic rabbits as defined in Article 2(3) of Council Directive 91/495/EEC(12);
(d) wild game as defined in Article 2(1)(a) of Council Directive 92/45/EEC(13).
(a) the third countries listed in Part 2 of Annex II, or parts of third countries set out in Part 1 of that Annex;
(b) the third countries listed in Parts 2 and 3 of Annex II or parts of third countries set out in Part 1 of that Annex.
(a) they shall come from the territory of a third country or a part thereof listed in Annex II and shall have undergone the minimum treatment for the import of meat products of the species concerned foreseen therein;
(b) they shall meet the specific animal health conditions for the species concerned set out in the model animal and public health certificate drawn up under Annex III;
(c) they shall be accompanied by an animal health certificate established in accordance with the model set out in Annex IV, signed by an official veterinarian of the competent veterinary services of the third country concerned;
(d) they shall be certified as acceptable for transit or storage (as appropriate) on the common veterinary entry document by the official veterinarian of the border inspection post of introduction into the Community.
(a) the consignment shall be sealed with a serially numbered seal by the official veterinarian of the competent authority at the border inspection post of introduction to the Community;
(b) the documents accompanying the consignment and referred to in Article 7 of Directive 97/78/EC shall be stamped ‘ONLY FOR TRANSIT TO RUSSIA VIA THE EC’ on each page by the official veterinarian of the competent authority of the border inspection post of introduction to the Community;
(c) the procedural requirements provided for in Article 11 of Directive 97/78/EC shall be complied with;
(d) the consignment shall be certified as acceptable for transit on the common veterinary entry document by the official veterinarian of the competent authority of the border inspection post of introduction to the Community.
(a) the meat products must:(i)contain meat and/or meat products derived from a single species or animal as set out under the relevant column in Parts 2 and 3 of Annex II indicating the species or animal concerned; and(ii)have been subjected to at least the specific treatment regime required for meat of that species or animal as set out in Part 4 of Annex II; or (i) contain meat and/or meat products derived from a single species or animal as set out under the relevant column in Parts 2 and 3 of Annex II indicating the species or animal concerned; and (ii) have been subjected to at least the specific treatment regime required for meat of that species or animal as set out in Part 4 of Annex II; or
(i) contain meat and/or meat products derived from a single species or animal as set out under the relevant column in Parts 2 and 3 of Annex II indicating the species or animal concerned; and
(ii) have been subjected to at least the specific treatment regime required for meat of that species or animal as set out in Part 4 of Annex II; or
(i) contain meat and/or meat products derived from a single species or animal as set out under the relevant column in Parts 2 and 3 of Annex II indicating the species or animal concerned; and
(ii) have been subjected to at least the specific treatment regime required for meat of that species or animal as set out in Part 4 of Annex II; or
(b) the meat products must:(i)contain fresh, processed or partly processed meat from more than one species or animal as set out under the relevant column of Parts 2 and 3 of Annex II which are mixed prior to undergoing their final treatment as set out in Part 4 of Annex II; and(ii)the final treatment referred to in (i) must be at least equal to the most severe treatment as set out in Part 4 of Annex II, for any of the individual meat constituents for the species or animal concerned as set out under the relevant column in Parts 2 and 3 of Annex II; or (i) contain fresh, processed or partly processed meat from more than one species or animal as set out under the relevant column of Parts 2 and 3 of Annex II which are mixed prior to undergoing their final treatment as set out in Part 4 of Annex II; and (ii) the final treatment referred to in (i) must be at least equal to the most severe treatment as set out in Part 4 of Annex II, for any of the individual meat constituents for the species or animal concerned as set out under the relevant column in Parts 2 and 3 of Annex II; or
(i) contain fresh, processed or partly processed meat from more than one species or animal as set out under the relevant column of Parts 2 and 3 of Annex II which are mixed prior to undergoing their final treatment as set out in Part 4 of Annex II; and
(ii) the final treatment referred to in (i) must be at least equal to the most severe treatment as set out in Part 4 of Annex II, for any of the individual meat constituents for the species or animal concerned as set out under the relevant column in Parts 2 and 3 of Annex II; or
(i) contain fresh, processed or partly processed meat from more than one species or animal as set out under the relevant column of Parts 2 and 3 of Annex II which are mixed prior to undergoing their final treatment as set out in Part 4 of Annex II; and
(ii) the final treatment referred to in (i) must be at least equal to the most severe treatment as set out in Part 4 of Annex II, for any of the individual meat constituents for the species or animal concerned as set out under the relevant column in Parts 2 and 3 of Annex II; or
(c) the final meat products must:(i)be prepared by the mixing of previously treated meat from more than one species or animal; and(ii)the previous treatment referred to in (i) which each constituent meat underwent must have been at least equal to the relevant treatment as set out in Part 4 of Annex II for the species or animal of the meat concerned as set out under the relevant column. (i) be prepared by the mixing of previously treated meat from more than one species or animal; and (ii) the previous treatment referred to in (i) which each constituent meat underwent must have been at least equal to the relevant treatment as set out in Part 4 of Annex II for the species or animal of the meat concerned as set out under the relevant column.
(i) be prepared by the mixing of previously treated meat from more than one species or animal; and
(ii) the previous treatment referred to in (i) which each constituent meat underwent must have been at least equal to the relevant treatment as set out in Part 4 of Annex II for the species or animal of the meat concerned as set out under the relevant column.
(i) be prepared by the mixing of previously treated meat from more than one species or animal; and
(ii) the previous treatment referred to in (i) which each constituent meat underwent must have been at least equal to the relevant treatment as set out in Part 4 of Annex II for the species or animal of the meat concerned as set out under the relevant column.
Country Territory Description of territory
Code Version
Argentina AR 01/2004 Whole country
AR-1 01/2004 The whole country except the provinces of Chubut, Santa Cruz and Tierra del Fuego
AR-2 01/2004 The provinces of Chubut, Santa Cruz and Tierra del Fuego
Bulgaria BG 01/2004 Whole country
BG-1 01/2004 As described in Annex II Part I to Council Decision 79/542/EEC(1)(as last amended)
BG-2 01/2004 As described in Annex II Part I to Decision 79/542/EEC (as last amended)
Brazil BR 01/2004 Whole country
BR-1 01/2004 As described in Annex I to Commission Decision 94/984/EC(2)(as last amended)
Serbia and Montenegro CS 01/2004 Whole country as described in Annex II Part I to Decision 79/542/EEC (as last amended)
Malaysia MY 01/2004 Whole country
MY-1 01/2004 Peninsular (Western) Malaysia only
Code ISO Country of origin or part thereof 1.Domestic bovine2.Farmed cloven-hoofed game-(excluding swine) 1. Domestic bovine 2. Farmed cloven-hoofed game-(excluding swine) Domestic ovine/ caprine 1.Domestic porcine2.Farmed cloven-hoofed game (swine) 1. Domestic porcine 2. Farmed cloven-hoofed game (swine) Domestic soliped 1.Domestic poultry2.Farmed feathered game 1. Domestic poultry 2. Farmed feathered game Domestic rabbit and farmed leporidae Wild cloven hoofed game (excluding swine) Wild swine Wild soliped Wild leporidae (rabbits and hares) Wild game birds Wild land mammalian game (excluding ungulates, solipeds and leporidae)
1. Domestic bovine
2. Farmed cloven-hoofed game-(excluding swine)
1. Domestic porcine
2. Farmed cloven-hoofed game (swine)
1. Domestic poultry
2. Farmed feathered game
AR Argentina AR C C C A A A C C XXX A D XXX
Argentina AR-1(3) C C C A A A C C XXX A D XXX
Argentina AR-2(3) A(4) A(4) C A A A C C XXX A D XXX
AU Australia A A A A D A A A XXX A D A
BG Bulgaria BG D D D A A A D D XXX A A XXX
Bulgaria BG-1 A A D A A A A D XXX A A XXX
Bulgaria BG-2 D D D A A A D D XXX A A XXX
BH Bahrain B B B B XXX A C C XXX A XXX XXX
BR Brazil C C C A D A C C XXX A D XXX
Brazil BR-1 C C C A A A C C XXX A A XXX
BW Botswana B B B B XXX A B B A A XXX XXX
BY Belarus C C C B XXX A C C XXX A XXX XXX
CA Canada A A A A A A A A XXX A A A
CH Switzerland A A A A A A A A XXX A A XXX
CL Chile A A A A A A B B XXX A A XXX
CN People’s Republic of China B B B B B A B B XXX A B XXX
CO Colombia B B B B XXX A B B XXX A XXX XXX
CS Serbia and Montenegro A A D A D A D D XXX A XXX XXX
ET Ethiopia B B B B XXX A B B XXX A XXX XXX
GL Greenland XXX XXX XXX XXX XXX A XXX XXX XXX A A A
HK Hong Kong B B B B D A B B XXX A XXX XXX
HR Croatia A A D A A A A D XXX A A XXX
IL Israel B B B B A A B B XXX A A XXX
IN India B B B B XXX A B B XXX A XXX XXX
IS Iceland B B B A A A B B XXX A A XXX
KE Kenya B B B B XXX A B B XXX A XXX XXX
KR Korea (Republic) XXX XXX XXX XXX D A XXX XXX XXX A D XXX
MA Morocco B B B B XXX A B B XXX A XXX XXX
MG Madagascar B B B B D A B B XXX A D XXX
MK Former Yugoslav Republic of Macedonia (Δ) A A B A XXX A B B XXX A XXX XXX
MU Mauritius B B B B XXX A B B XXX A XXX XXX
MX Mexico A D D A D A D D XXX A D XXX
MY Malaysia MY XXX XXX XXX XXX XXX XXX XXX XXX XXX XXX XXX XXX
Malaysia MY-1 XXX XXX XXX XXX D A XXX XXX XXX A D XXX
NA Namibia(3) B B B B D A B B A A D XXX
NZ New Zealand A A A A A A A A XXX A A A
PY Paraguay C C C B XXX A C C XXX A XXX XXX
RO Romania A A D A A A A D XXX A A A
RU Russia C C C B XXX A C C XXX A XXX A
SG Singapore B B B B D A B B XXX A XXX XXX
SZ Swaziland B B B B XXX A B B A A XXX XXX
TH Thailand B B B B A A B B XXX A D XXX
TN Tunisia C C B B A A B B XXX A D XXX
TR Turkey XXX XXX XXX XXX D A XXX XXX XXX A D XXX
UA Ukraine XXX XXX XXX XXX XXX A XXX XXX XXX A XXX XXX
US United States of America A A A A A A A A XXX A A XXX
UY Uruguay C C B A D A XXX XXX XXX A D XXX
ZA South Africa(3) C C C A D A C C A A D XXX
ZW Zimbabwe(3) C C B A D A B B XXX A D XXX
(Δ)Former Yugoslav Republic of Macedonia: provisional code that does not affect the definitive denomination of the country to be attributed after the conclusion of the negotiations currently taking place in the United Nations.XXXNo certificate laid down and meat products containing meat of this species are not authorised. (Δ) Former Yugoslav Republic of Macedonia: provisional code that does not affect the definitive denomination of the country to be attributed after the conclusion of the negotiations currently taking place in the United Nations. XXX No certificate laid down and meat products containing meat of this species are not authorised.
(Δ) Former Yugoslav Republic of Macedonia: provisional code that does not affect the definitive denomination of the country to be attributed after the conclusion of the negotiations currently taking place in the United Nations.
XXX No certificate laid down and meat products containing meat of this species are not authorised.
1. Domestic bovine
2. Farmed cloven-hoofed game-(excluding swine)
1. Domestic porcine
2. Farmed cloven-hoofed game (swine)
1. Domestic poultry
2. Farmed feathered game
(Δ) Former Yugoslav Republic of Macedonia: provisional code that does not affect the definitive denomination of the country to be attributed after the conclusion of the negotiations currently taking place in the United Nations.
XXX No certificate laid down and meat products containing meat of this species are not authorised.
ISO Code Country of origin or part thereof 1.Domestic bovine2.Farmed cloven hoofed game excluding swine 1. Domestic bovine 2. Farmed cloven hoofed game excluding swine Domestic ovine/caprine 1.Domestic porcine2.Farmed cloven-hoofed game (swine) 1. Domestic porcine 2. Farmed cloven-hoofed game (swine) Domestic soliped 1.Domestic poultry2.Farmed feathered game 1. Domestic poultry 2. Farmed feathered game Domestic rabbit and farmed leporidae Wild cloven hoofed game (excluding swine) Wild swine Wild soliped Wild leporidae (rabbits and hares) Wild game birds Wild land mammalian game (excluding ungulates, solipeds and leporidae)
1. Domestic bovine
2. Farmed cloven hoofed game excluding swine
1. Domestic porcine
2. Farmed cloven-hoofed game (swine)
1. Domestic poultry
2. Farmed feathered game
AR Argentina F F XXX XXX XXX A XXX XXX XXX A XXX XXX
NA Namibia E E XXX XXX E A XXX XXX A A E XXX
ZA South Africa E E XXX XXX E A XXX XXX A A E XXX
ZW Zimbabwe E E XXX XXX E A XXX XXX E A E XXX
1. Domestic bovine
2. Farmed cloven hoofed game excluding swine
1. Domestic porcine
2. Farmed cloven-hoofed game (swine)
1. Domestic poultry
2. Farmed feathered game
A = No minimum specified temperature or other treatment is established for animal health purposes for the meat product. However, the meat must have undergone a treatment such that its cut surface shows that it no longer has the characteristics of fresh meat and the fresh meat used must also satisfy the animal health rules applicable to the export of fresh meat to the Community.
B = Treatment in a hermetically sealed container to an Fovalue of three or more.
C = A minimum temperature of 80 °C which must be reached throughout the meat during the processing of the meat product.
D = A minimum temperature of 70 °C which must be reached throughout the meat during the processing of meat products, or for raw ham, a treatment consisting of natural fermentation and maturation of not less than nine months and resulting in the following characteristics:—Awvalue of not more than 0,93,—pH value of not more than 6,0. — Awvalue of not more than 0,93, — pH value of not more than 6,0.
— Awvalue of not more than 0,93,
— pH value of not more than 6,0.
E = In the case of ‘biltong’ type products, a treatment to achieve:—Awvalue of not more than 0,93,—pH value of not more than 6,0. — Awvalue of not more than 0,93, — pH value of not more than 6,0.
— Awvalue of not more than 0,93,
— pH value of not more than 6,0.
F = A heat treatment ensuring that a centre temperature of at least 65 °C is reached for a period of time as necessary to achieve a pasteurisation value (pv) equal to or above 40.
— Awvalue of not more than 0,93,
— pH value of not more than 6,0.
— Awvalue of not more than 0,93,
— pH value of not more than 6,0.
THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Council Directive 92/118/EEC of 17 December 1992, laying down animal health and public health requirements governing trade in and imports into the Community of products not subject to the said requirements laid down in specific Community rules referred to in Annex A(1) to Directive 89/662/EEC and, as regards pathogens, to Directive 90/425/EEC(1), and in particular Article 10(2)(c) thereof,
Having regard to Council Directive 2002/99/EC of 16 December 2002 laying down the animal health rules governing the production, processing, distribution and introduction of products of animal origin for human consumption(2), and in particular the introductory phrase of Article 8, the first paragraph of Article 8(1), Article 8(4), Article 9(2)(b), Article 9(4)(b) and (c) thereof,
(1) Commission Decision 97/41/EC of 18 December 1996 establishing health conditions and a public health certificate for the importation from third countries of meat products obtained from poultry meat, farmed game meat, wild game meat, and rabbit meat(3)lays down public health conditions for the importation into the Community of certain meat products.
(2) Commission Decision 97/221/EC of 28 February 1997 laying down the animal health conditions and model veterinary certificates in respect of imports of meat products from third countries and revoking Decision 91/449/EEC(4)lays down animal health conditions and certification rules for the importation into the Community of certain meat products.
(3) Commission Decision 97/222/EC of 28 February 1997 laying down the list of third countries from which the Member States authorise the importation of meat products(5)provides for the importation into the Community of certain meat products provided that such products have undergone the appropriate treatment and comply with Community veterinary certification requirements.
(4) Council Directive 72/462/EEC of 12 December 1972 on health and veterinary inspection problems upon importation of bovine, ovine and caprine animals and swine, fresh meat or meat products from third countries(6)lays down animal health requirements for the importation into the Community of certain meat products. Council Directive 2004/68/EC(7)provides for the repeal of Directive 72/462/EEC from 1 January 2006.
(5) Directive 2002/99/EC lays down the animal health rules governing the production, processing, distribution and introduction of products of animal origin for human consumption. That Directive is to be implemented by the Member States before 1 January 2005.
(6) Council Directive 77/99/EEC of 21 December 1976 on health problems affecting the production and marketing of meat products and certain other products of animal origin(8)will be in force till 1 January 2006 when it will be repealed and any definition of meat based products in acts adopted before 1 January 2006 must refer to Directive 77/99/EEC.
(7) In view of the entry into force of Directive 2002/99/EC, it is necessary to amend and update Community public and animal health conditions and certification requirements for the importation into the Community of meat products derived from domestic bovines, porcines, ovines, caprines, equidae, poultry, farmed game, domestic rabbits and wild game.
(8) In addition, in the interests of clarity and consistency of Community legislation, it is appropriate to lay down the public and animal health conditions in a single model health certificate for importation of meat products into the Community.
(9) Due to differences in the animal health situation in third countries, it is appropriate to lay down rules concerning treatments for meat products from third countries or parts of third countries prior to their importation into the Community.
(10) In the interests of clarity and consistency of Community legislation, it is appropriate to repeal Decisions 97/41/EC, 97/221/EC and 97/222/EC and replace them by this Decision. Accordingly, this Decision should contain the animal and public health conditions and certification requirements, together with the list of third countries and the treatments required for the importation of various categories of meat products into the Community.
(11) Health conditions and veterinary certification should apply without prejudice to the requirement of Commission Decision 2004/432/EC of 29 April 2004 on the approval of residue monitoring plans submitted by third countries in accordance with Directive 96/23/EC(9).
(12) Council Directive 97/78/EC of 18 December 1997 laying down the principles governing the organisation of veterinary checks on products entering the Community from third countries(10)lays down rules concerning veterinary checks on animal products introduced into the Community from third countries for the importation and transit of products of animal origin in the Community, including certain certification requirements.
(13) In the interests of animal and public health and in order to prevent the spread of animal diseases in the Community, a new specific model public and animal health certificate should be established in this Decision. In addition, it should be provided that transit through the Community of consignments of meat products is only permitted where those products come from third countries or parts of third countries whose products are not prohibited for introduction into the Community.
(14) It is necessary to lay down specific conditions for transit via the Community of consignments of meat products to and from Russia due to the geographical situation of Kaliningrad and taking into account climatic problems impeding the use of some ports at certain times of the year.
(15) Commission Decision 2001/881/EC of 7 December 2001 drawing up a list of border inspection posts agreed for veterinary checks on animals and animal products from third countries and updating the detailed rules concerning the checks to be carried out by the experts of the Commission(11), specifies the Border Inspection Posts authorised to control the transit of consignments of meat products to and from Russia via the Community
(16) The treatments provided for poultry meat products originating in Bulgaria and Israel and for wild swine meat products originating in Switzerland should be reviewed in order to bring them into line with the current import conditions for fresh meat of the concerned species from those countries.
(17) The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health,
HAS ADOPTED THIS DECISION:

Subject matter and scope
Article 1
1. This Decision lays down animal and public health rules for the importation into the Community of consignments of certain meat products, including the lists of third countries and parts of third countries from which the importation of such products shall be authorised, the model public and animal health certificates and rules on treatments required for those products.
2. This Decision shall apply without prejudice to Decision 2004/432/EC.

Definition of meat products
Article 2
For the purposes of this Decision, the definition of meat products as laid down in Article 2(a) of Directive 77/99/EEC shall apply.

Conditions concerning species and animals
Article 3
Member States shall ensure that consignments of meat products imported into the Community are derived from meat or meat products from the following species or animals:
(a)
domestic poultry of the following species: domestic fowl, turkeys, guinea fowl, geese and ducks;
(b)
domestic animals of the following species: bovine animals, includingBubalus bubalis, Bison bison, swine, sheep, goats and solipeds;
(c)
farmed game and domestic rabbits as defined in Article 2(3) of Council Directive 91/495/EEC(12);
(d)
wild game as defined in Article 2(1)(a) of Council Directive 92/45/EEC(13).

Animal health conditions concerning the origin and treatment of the meat products
Article 4
Subject to compliance with the conditions concerning the origin and treatment of the meat products, as set out in Annex I, Member States shall authorise the importation of meat products originating in the following third countries or parts of third countries:
(a)
the third countries listed in Part 2 of Annex II, or parts of third countries set out in Part 1 of that Annex;
(b)
the third countries listed in Parts 2 and 3 of Annex II or parts of third countries set out in Part 1 of that Annex.

Public health conditions concerning the fresh meat used in the production of the meat products to be imported into the Community
Article 5
Member States shall authorise import of meat products obtained from fresh meat that complies with the Community public health requirements for the importation of such meat into the Community.

Animal and public health certificates
Article 6
Consignments of meat products shall comply with the requirements of the model public and animal health certificate set out in Annex III.
That certificate shall accompany the consignment of meat products and be duly completed and signed by the official veterinarian of the third country of dispatch.

Consignments of meat products in transit or storage in the Community
Article 7
Member States shall ensure that consignments of meat products, introduced into the Community and which are destined for a third country either by transit immediately or after storage in accordance with Article 12(4) or 13 of Directive 97/78/EC, and not intended for importation into the Community, shall comply with the following requirements:
(a)
they shall come from the territory of a third country or a part thereof listed in Annex II and shall have undergone the minimum treatment for the import of meat products of the species concerned foreseen therein;
(b)
they shall meet the specific animal health conditions for the species concerned set out in the model animal and public health certificate drawn up under Annex III;
(c)
they shall be accompanied by an animal health certificate established in accordance with the model set out in Annex IV, signed by an official veterinarian of the competent veterinary services of the third country concerned;
(d)
they shall be certified as acceptable for transit or storage (as appropriate) on the common veterinary entry document by the official veterinarian of the border inspection post of introduction into the Community.

Derogation for certain destinations in Russia
Article 8
1. By way of derogation from Article 7, Member States shall authorise the transit by road or by rail through the Community, between designated Community border inspection posts listed in Annex to Decision 2001/881/EC, of consignments of meat products coming from and destined to Russia directly or via another third country provided that they comply with the following requirements:
(a)
the consignment shall be sealed with a serially numbered seal by the official veterinarian of the competent authority at the border inspection post of introduction to the Community;
(b)
the documents accompanying the consignment and referred to in Article 7 of Directive 97/78/EC shall be stamped ‘ONLY FOR TRANSIT TO RUSSIA VIA THE EC’ on each page by the official veterinarian of the competent authority of the border inspection post of introduction to the Community;
(c)
the procedural requirements provided for in Article 11 of Directive 97/78/EC shall be complied with;
(d)
the consignment shall be certified as acceptable for transit on the common veterinary entry document by the official veterinarian of the competent authority of the border inspection post of introduction to the Community.
2. Member States shall not authorise the unloading or storage, as defined in Article 12(4) or Article 13 of Directive 97/78/EC, in the Community of such consignments.
3. Member States shall ensure that the competent authority makes regular audits to ensure that the number of consignments and the quantities of products leaving the Community matches the number and quantities entering.

Transitional provisions
Article 9
Member States shall authorise the importation into the Community of consignments of meat products certified in accordance with the model veterinary certificates laid down in Decisions 97/41/EEC or 97/221/EEC for a period of six months from 17 June 2005.

Repeals
Article 10
Decisions 97/41/EC, 97/221/EC and 97/222/EC are repealed.

Date of application
Article 11
This Decision shall apply from 17 June 2005.

Addresses
Article 12
This Decision is addressed to the Member States.

THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Council Directive 92/118/EEC of 17 December 1992, laying down animal health and public health requirements governing trade in and imports into the Community of products not subject to the said requirements laid down in specific Community rules referred to in Annex A(1) to Directive 89/662/EEC and, as regards pathogens, to Directive 90/425/EEC(1), and in particular Article 10(2)(c) thereof,
Having regard to Council Directive 2002/99/EC of 16 December 2002 laying down the animal health rules governing the production, processing, distribution and introduction of products of animal origin for human consumption(2), and in particular the introductory phrase of Article 8, the first paragraph of Article 8(1), Article 8(4), Article 9(2)(b), Article 9(4)(b) and (c) thereof,
(1) Commission Decision 97/41/EC of 18 December 1996 establishing health conditions and a public health certificate for the importation from third countries of meat products obtained from poultry meat, farmed game meat, wild game meat, and rabbit meat(3)lays down public health conditions for the importation into the Community of certain meat products.
(2) Commission Decision 97/221/EC of 28 February 1997 laying down the animal health conditions and model veterinary certificates in respect of imports of meat products from third countries and revoking Decision 91/449/EEC(4)lays down animal health conditions and certification rules for the importation into the Community of certain meat products.
(3) Commission Decision 97/222/EC of 28 February 1997 laying down the list of third countries from which the Member States authorise the importation of meat products(5)provides for the importation into the Community of certain meat products provided that such products have undergone the appropriate treatment and comply with Community veterinary certification requirements.
(4) Council Directive 72/462/EEC of 12 December 1972 on health and veterinary inspection problems upon importation of bovine, ovine and caprine animals and swine, fresh meat or meat products from third countries(6)lays down animal health requirements for the importation into the Community of certain meat products. Council Directive 2004/68/EC(7)provides for the repeal of Directive 72/462/EEC from 1 January 2006.
(5) Directive 2002/99/EC lays down the animal health rules governing the production, processing, distribution and introduction of products of animal origin for human consumption. That Directive is to be implemented by the Member States before 1 January 2005.
(6) Council Directive 77/99/EEC of 21 December 1976 on health problems affecting the production and marketing of meat products and certain other products of animal origin(8)will be in force till 1 January 2006 when it will be repealed and any definition of meat based products in acts adopted before 1 January 2006 must refer to Directive 77/99/EEC.
(7) In view of the entry into force of Directive 2002/99/EC, it is necessary to amend and update Community public and animal health conditions and certification requirements for the importation into the Community of meat products derived from domestic bovines, porcines, ovines, caprines, equidae, poultry, farmed game, domestic rabbits and wild game.
(8) In addition, in the interests of clarity and consistency of Community legislation, it is appropriate to lay down the public and animal health conditions in a single model health certificate for importation of meat products into the Community.
(9) Due to differences in the animal health situation in third countries, it is appropriate to lay down rules concerning treatments for meat products from third countries or parts of third countries prior to their importation into the Community.
(10) In the interests of clarity and consistency of Community legislation, it is appropriate to repeal Decisions 97/41/EC, 97/221/EC and 97/222/EC and replace them by this Decision. Accordingly, this Decision should contain the animal and public health conditions and certification requirements, together with the list of third countries and the treatments required for the importation of various categories of meat products into the Community.
(11) Health conditions and veterinary certification should apply without prejudice to the requirement of Commission Decision 2004/432/EC of 29 April 2004 on the approval of residue monitoring plans submitted by third countries in accordance with Directive 96/23/EC(9).
(12) Council Directive 97/78/EC of 18 December 1997 laying down the principles governing the organisation of veterinary checks on products entering the Community from third countries(10)lays down rules concerning veterinary checks on animal products introduced into the Community from third countries for the importation and transit of products of animal origin in the Community, including certain certification requirements.
(13) In the interests of animal and public health and in order to prevent the spread of animal diseases in the Community, a new specific model public and animal health certificate should be established in this Decision. In addition, it should be provided that transit through the Community of consignments of meat products is only permitted where those products come from third countries or parts of third countries whose products are not prohibited for introduction into the Community.
(14) It is necessary to lay down specific conditions for transit via the Community of consignments of meat products to and from Russia due to the geographical situation of Kaliningrad and taking into account climatic problems impeding the use of some ports at certain times of the year.
(15) Commission Decision 2001/881/EC of 7 December 2001 drawing up a list of border inspection posts agreed for veterinary checks on animals and animal products from third countries and updating the detailed rules concerning the checks to be carried out by the experts of the Commission(11), specifies the Border Inspection Posts authorised to control the transit of consignments of meat products to and from Russia via the Community
(16) The treatments provided for poultry meat products originating in Bulgaria and Israel and for wild swine meat products originating in Switzerland should be reviewed in order to bring them into line with the current import conditions for fresh meat of the concerned species from those countries.
(17) The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health,
HAS ADOPTED THIS DECISION:

Subject matter and scope

1. This Decision lays down animal and public health rules for the importation into the Community of consignments of certain meat products, including the lists of third countries and parts of third countries from which the importation of such products shall be authorised, the model public and animal health certificates and rules on treatments required for those products.
2. This Decision shall apply without prejudice to Decision 2004/432/EC.

Definition of meat products

For the purposes of this Decision, the definition of meat products as laid down in Article 2(a) of Directive 77/99/EEC shall apply.

Conditions concerning species and animals

Member States shall ensure that consignments of meat products imported into the Community are derived from meat or meat products from the following species or animals:
(a)
domestic poultry of the following species: domestic fowl, turkeys, guinea fowl, geese and ducks;
(b)
domestic animals of the following species: bovine animals, includingBubalus bubalis, Bison bison, swine, sheep, goats and solipeds;
(c)
farmed game and domestic rabbits as defined in Article 2(3) of Council Directive 91/495/EEC(12);
(d)
wild game as defined in Article 2(1)(a) of Council Directive 92/45/EEC(13).

Animal health conditions concerning the origin and treatment of the meat products

Subject to compliance with the conditions concerning the origin and treatment of the meat products, as set out in Annex I, Member States shall authorise the importation of meat products originating in the following third countries or parts of third countries:
(a)
the third countries listed in Part 2 of Annex II, or parts of third countries set out in Part 1 of that Annex;
(b)
the third countries listed in Parts 2 and 3 of Annex II or parts of third countries set out in Part 1 of that Annex.

Public health conditions concerning the fresh meat used in the production of the meat products to be imported into the Community

Member States shall authorise import of meat products obtained from fresh meat that complies with the Community public health requirements for the importation of such meat into the Community.

Animal and public health certificates

Consignments of meat products shall comply with the requirements of the model public and animal health certificate set out in Annex III.
That certificate shall accompany the consignment of meat products and be duly completed and signed by the official veterinarian of the third country of dispatch.

Consignments of meat products in transit or storage in the Community

Member States shall ensure that consignments of meat products, introduced into the Community and which are destined for a third country either by transit immediately or after storage in accordance with Article 12(4) or 13 of Directive 97/78/EC, and not intended for importation into the Community, shall comply with the following requirements:
(a)
they shall come from the territory of a third country or a part thereof listed in Annex II and shall have undergone the minimum treatment for the import of meat products of the species concerned foreseen therein;
(b)
they shall meet the specific animal health conditions for the species concerned set out in the model animal and public health certificate drawn up under Annex III;
(c)
they shall be accompanied by an animal health certificate established in accordance with the model set out in Annex IV, signed by an official veterinarian of the competent veterinary services of the third country concerned;
(d)
they shall be certified as acceptable for transit or storage (as appropriate) on the common veterinary entry document by the official veterinarian of the border inspection post of introduction into the Community.

Derogation for certain destinations in Russia

1. By way of derogation from Article 7, Member States shall authorise the transit by road or by rail through the Community, between designated Community border inspection posts listed in Annex to Decision 2001/881/EC, of consignments of meat products coming from and destined to Russia directly or via another third country provided that they comply with the following requirements:
(a)
the consignment shall be sealed with a serially numbered seal by the official veterinarian of the competent authority at the border inspection post of introduction to the Community;
(b)
the documents accompanying the consignment and referred to in Article 7 of Directive 97/78/EC shall be stamped ‘ONLY FOR TRANSIT TO RUSSIA VIA THE EC’ on each page by the official veterinarian of the competent authority of the border inspection post of introduction to the Community;
(c)
the procedural requirements provided for in Article 11 of Directive 97/78/EC shall be complied with;
(d)
the consignment shall be certified as acceptable for transit on the common veterinary entry document by the official veterinarian of the competent authority of the border inspection post of introduction to the Community.
2. Member States shall not authorise the unloading or storage, as defined in Article 12(4) or Article 13 of Directive 97/78/EC, in the Community of such consignments.
3. Member States shall ensure that the competent authority makes regular audits to ensure that the number of consignments and the quantities of products leaving the Community matches the number and quantities entering.

Transitional provisions

Member States shall authorise the importation into the Community of consignments of meat products certified in accordance with the model veterinary certificates laid down in Decisions 97/41/EEC or 97/221/EEC for a period of six months from 17 June 2005.

Repeals

Decisions 97/41/EC, 97/221/EC and 97/222/EC are repealed.

Date of application

This Decision shall apply from 17 June 2005.

Addresses

This Decision is addressed to the Member States.
ANNEX I 1.
Meat products originating in the third countries or parts of third countries referred to in Article 4(a) shall contain meat eligible for importation into the Community as fresh meat and/or meat products derived from one or more of the species or animals which have undergone a non-specific treatment as set out in Part 4 of Annex II.
2.
Meat products originating in third countries or parts of third countries referred to in Article 4(b) shall comply with the following conditions set out in either (a), (b) or (c):
(a) the meat products must:
(i) contain meat and/or meat products derived from a single species or animal as set out under the relevant column in Parts 2 and 3 of Annex II indicating the species or animal concerned; and
(ii) have been subjected to at least the specific treatment regime required for meat of that species or animal as set out in Part 4 of Annex II; or
(b) the meat products must:
(i) contain fresh, processed or partly processed meat from more than one species or animal as set out under the relevant column of Parts 2 and 3 of Annex II which are mixed prior to undergoing their final treatment as set out in Part 4 of Annex II; and
(ii) the final treatment referred to in (i) must be at least equal to the most severe treatment as set out in Part 4 of Annex II, for any of the individual meat constituents for the species or animal concerned as set out under the relevant column in Parts 2 and 3 of Annex II; or
(c) the final meat products must:
(i) be prepared by the mixing of previously treated meat from more than one species or animal; and
(ii) the previous treatment referred to in (i) which each constituent meat underwent must have been at least equal to the relevant treatment as set out in Part 4 of Annex II for the species or animal of the meat concerned as set out under the relevant column.
3.
The treatments set out in Part 4 of Annex II shall be the minimum acceptable processing conditions for animal health purposes for meat derived from the species or animal concerned originating in the third countries or parts of third countries listed in Annex II.

PART 1

ANNEX IIDescription of regionalised territories as laid down for the countries listed in parts 2 and 3
Country | Territory | Description of territory
Code | Version
Argentina | AR | 01/2004 | Whole country
AR-1 | 01/2004 | The whole country except the provinces of Chubut, Santa Cruz and Tierra del Fuego
AR-2 | 01/2004 | The provinces of Chubut, Santa Cruz and Tierra del Fuego
Bulgaria | BG | 01/2004 | Whole country
BG-1 | 01/2004 | As described in Annex II Part I to Council Decision 79/542/EEC(1)(as last amended)
BG-2 | 01/2004 | As described in Annex II Part I to Decision 79/542/EEC (as last amended)
Brazil | BR | 01/2004 | Whole country
BR-1 | 01/2004 | As described in Annex I to Commission Decision 94/984/EC(2)(as last amended)
Serbia and Montenegro | CS | 01/2004 | Whole country as described in Annex II Part I to Decision 79/542/EEC (as last amended)
Malaysia | MY | 01/2004 | Whole country
MY-1 | 01/2004 | Peninsular (Western) Malaysia onlyPART 2Third countries or parts thereof from which meat products are authorised for importation into the Community
Code ISO | Country of origin or part thereof | 1.Domestic bovine2.Farmed cloven-hoofed game-(excluding swine) | 1. | Domestic bovine | 2. | Farmed cloven-hoofed game-(excluding swine) | Domestic ovine/ caprine | 1.Domestic porcine2.Farmed cloven-hoofed game (swine) | 1. | Domestic porcine | 2. | Farmed cloven-hoofed game (swine) | Domestic soliped | 1.Domestic poultry2.Farmed feathered game | 1. | Domestic poultry | 2. | Farmed feathered game | Domestic rabbit and farmed leporidae | Wild cloven hoofed game (excluding swine) | Wild swine | Wild soliped | Wild leporidae (rabbits and hares) | Wild game birds | Wild land mammalian game (excluding ungulates, solipeds and leporidae)
1. | Domestic bovine
2. | Farmed cloven-hoofed game-(excluding swine)
1. | Domestic porcine
2. | Farmed cloven-hoofed game (swine)
1. | Domestic poultry
2. | Farmed feathered game
AR | Argentina AR | C | C | C | A | A | A | C | C | XXX | A | D | XXX
Argentina AR-1(3) | C | C | C | A | A | A | C | C | XXX | A | D | XXX
Argentina AR-2(3) | A(4) | A(4) | C | A | A | A | C | C | XXX | A | D | XXX
AU | Australia | A | A | A | A | D | A | A | A | XXX | A | D | A
BG | Bulgaria BG | D | D | D | A | A | A | D | D | XXX | A | A | XXX
Bulgaria BG-1 | A | A | D | A | A | A | A | D | XXX | A | A | XXX
Bulgaria BG-2 | D | D | D | A | A | A | D | D | XXX | A | A | XXX
BH | Bahrain | B | B | B | B | XXX | A | C | C | XXX | A | XXX | XXX
BR | Brazil | C | C | C | A | D | A | C | C | XXX | A | D | XXX
Brazil BR-1 | C | C | C | A | A | A | C | C | XXX | A | A | XXX
BW | Botswana | B | B | B | B | XXX | A | B | B | A | A | XXX | XXX
BY | Belarus | C | C | C | B | XXX | A | C | C | XXX | A | XXX | XXX
CA | Canada | A | A | A | A | A | A | A | A | XXX | A | A | A
CH | Switzerland | A | A | A | A | A | A | A | A | XXX | A | A | XXX
CL | Chile | A | A | A | A | A | A | B | B | XXX | A | A | XXX
CN | People’s Republic of China | B | B | B | B | B | A | B | B | XXX | A | B | XXX
CO | Colombia | B | B | B | B | XXX | A | B | B | XXX | A | XXX | XXX
CS | Serbia and Montenegro | A | A | D | A | D | A | D | D | XXX | A | XXX | XXX
ET | Ethiopia | B | B | B | B | XXX | A | B | B | XXX | A | XXX | XXX
GL | Greenland | XXX | XXX | XXX | XXX | XXX | A | XXX | XXX | XXX | A | A | A
HK | Hong Kong | B | B | B | B | D | A | B | B | XXX | A | XXX | XXX
HR | Croatia | A | A | D | A | A | A | A | D | XXX | A | A | XXX
IL | Israel | B | B | B | B | A | A | B | B | XXX | A | A | XXX
IN | India | B | B | B | B | XXX | A | B | B | XXX | A | XXX | XXX
IS | Iceland | B | B | B | A | A | A | B | B | XXX | A | A | XXX
KE | Kenya | B | B | B | B | XXX | A | B | B | XXX | A | XXX | XXX
KR | Korea (Republic) | XXX | XXX | XXX | XXX | D | A | XXX | XXX | XXX | A | D | XXX
MA | Morocco | B | B | B | B | XXX | A | B | B | XXX | A | XXX | XXX
MG | Madagascar | B | B | B | B | D | A | B | B | XXX | A | D | XXX
MK | Former Yugoslav Republic of Macedonia (Δ) | A | A | B | A | XXX | A | B | B | XXX | A | XXX | XXX
MU | Mauritius | B | B | B | B | XXX | A | B | B | XXX | A | XXX | XXX
MX | Mexico | A | D | D | A | D | A | D | D | XXX | A | D | XXX
MY | Malaysia MY | XXX | XXX | XXX | XXX | XXX | XXX | XXX | XXX | XXX | XXX | XXX | XXX
Malaysia MY-1 | XXX | XXX | XXX | XXX | D | A | XXX | XXX | XXX | A | D | XXX
NA | Namibia(3) | B | B | B | B | D | A | B | B | A | A | D | XXX
NZ | New Zealand | A | A | A | A | A | A | A | A | XXX | A | A | A
PY | Paraguay | C | C | C | B | XXX | A | C | C | XXX | A | XXX | XXX
RO | Romania | A | A | D | A | A | A | A | D | XXX | A | A | A
RU | Russia | C | C | C | B | XXX | A | C | C | XXX | A | XXX | A
SG | Singapore | B | B | B | B | D | A | B | B | XXX | A | XXX | XXX
SZ | Swaziland | B | B | B | B | XXX | A | B | B | A | A | XXX | XXX
TH | Thailand | B | B | B | B | A | A | B | B | XXX | A | D | XXX
TN | Tunisia | C | C | B | B | A | A | B | B | XXX | A | D | XXX
TR | Turkey | XXX | XXX | XXX | XXX | D | A | XXX | XXX | XXX | A | D | XXX
UA | Ukraine | XXX | XXX | XXX | XXX | XXX | A | XXX | XXX | XXX | A | XXX | XXX
US | United States of America | A | A | A | A | A | A | A | A | XXX | A | A | XXX
UY | Uruguay | C | C | B | A | D | A | XXX | XXX | XXX | A | D | XXX
ZA | South Africa(3) | C | C | C | A | D | A | C | C | A | A | D | XXX
ZW | Zimbabwe(3) | C | C | B | A | D | A | B | B | XXX | A | D | XXX
(Δ)Former Yugoslav Republic of Macedonia: provisional code that does not affect the definitive denomination of the country to be attributed after the conclusion of the negotiations currently taking place in the United Nations.XXXNo certificate laid down and meat products containing meat of this species are not authorised. | (Δ) | Former Yugoslav Republic of Macedonia: provisional code that does not affect the definitive denomination of the country to be attributed after the conclusion of the negotiations currently taking place in the United Nations. | XXX | No certificate laid down and meat products containing meat of this species are not authorised.
(Δ) | Former Yugoslav Republic of Macedonia: provisional code that does not affect the definitive denomination of the country to be attributed after the conclusion of the negotiations currently taking place in the United Nations.
XXX | No certificate laid down and meat products containing meat of this species are not authorised.PART 3Third countries or parts thereof not authorised under the non specific treatment regime (A) but from where biltong/jerky or pasteurised meat products are authorised for importation into the Community
ISO Code | Country of origin or part thereof | 1.Domestic bovine2.Farmed cloven hoofed game excluding swine | 1. | Domestic bovine | 2. | Farmed cloven hoofed game excluding swine | Domestic ovine/caprine | 1.Domestic porcine2.Farmed cloven-hoofed game (swine) | 1. | Domestic porcine | 2. | Farmed cloven-hoofed game (swine) | Domestic soliped | 1.Domestic poultry2.Farmed feathered game | 1. | Domestic poultry | 2. | Farmed feathered game | Domestic rabbit and farmed leporidae | Wild cloven hoofed game (excluding swine) | Wild swine | Wild soliped | Wild leporidae (rabbits and hares) | Wild game birds | Wild land mammalian game (excluding ungulates, solipeds and leporidae)
1. | Domestic bovine
2. | Farmed cloven hoofed game excluding swine
1. | Domestic porcine
2. | Farmed cloven-hoofed game (swine)
1. | Domestic poultry
2. | Farmed feathered game
AR | Argentina | F | F | XXX | XXX | XXX | A | XXX | XXX | XXX | A | XXX | XXX
NA | Namibia | E | E | XXX | XXX | E | A | XXX | XXX | A | A | E | XXX
ZA | South Africa | E | E | XXX | XXX | E | A | XXX | XXX | A | A | E | XXX
ZW | Zimbabwe | E | E | XXX | XXX | E | A | XXX | XXX | E | A | E | XXXPART 4Interpretation of codes used in tables in parts 2 and 3TREATMENTS REFERRED TO IN ANNEX INon-specific treatment regime:
A | = | No minimum specified temperature or other treatment is established for animal health purposes for the meat product. However, the meat must have undergone a treatment such that its cut surface shows that it no longer has the characteristics of fresh meat and the fresh meat used must also satisfy the animal health rules applicable to the export of fresh meat to the Community.Specific treatment regimes — listed in descending order of severity:
B | = | Treatment in a hermetically sealed container to an Fovalue of three or more.
C | = | A minimum temperature of 80 °C which must be reached throughout the meat during the processing of the meat product.
D | = | A minimum temperature of 70 °C which must be reached throughout the meat during the processing of meat products, or for raw ham, a treatment consisting of natural fermentation and maturation of not less than nine months and resulting in the following characteristics:—Awvalue of not more than 0,93,—pH value of not more than 6,0. | — | Awvalue of not more than 0,93, | — | pH value of not more than 6,0.
— | Awvalue of not more than 0,93,
— | pH value of not more than 6,0.
E | = | In the case of ‘biltong’ type products, a treatment to achieve:—Awvalue of not more than 0,93,—pH value of not more than 6,0. | — | Awvalue of not more than 0,93, | — | pH value of not more than 6,0.
— | Awvalue of not more than 0,93,
— | pH value of not more than 6,0.
F | = | A heat treatment ensuring that a centre temperature of at least 65 °C is reached for a period of time as necessary to achieve a pasteurisation value (pv) equal to or above 40.
(1)
OJ L 146, 14.6.1979, p. 15.
(2)
OJ L 378, 31.12.1994, p. 11.
(3) See Part 3 of this Annex for the minimum treatment requirements applicable to pasteurised meat products and biltong.
(4) For meat products prepared from fresh meat obtained from animals slaughtered after 1 March 2002.
ANNEX III(Model animal and public health certificate for meat products intended for consignment to the European Community from third countries) (*1)

Model ‘MEAT PRODUCTS’
1. Consignor (name and address in full)
VETERINARY CERTIFICATE
for meat products (1), into the European Community No (2) ORIGINAL 3. Origin of the meat product (3) 2. Consignee (name and address in full)
3.1. Country:
3.2. Code of territory: 4. Competent Authority
4.1. Ministry:
4.2. Service: 5. Intended destination of the meat product
5.1. EU Member State:
4.3. Local/Regional level:
5.2. Establishment:
Name and address: 6. Address(es) and veterinary approval number of: (6) Approval or registration number (where applicable):
6.1. Establishment(s) supplying fresh meat: 7. Means of transport and consignment identification (4) 6.2. Meat product establishment:
7.1. [Lorry]/[Rail-wagon]/[Ship]/[Aircraft] (5) 7.2. Registration number(s), ship name or flight number: (4) 6.3. Storage establishment: 8. Identification of the meat product
8.1. Indicate the species of origin of the meat(s) used in the meat product (animal species) (7):
Domestic species: Bovine Ovine Caprine Porcine Soliped
Poultry specify
Farmed game: Cloven hoofed (excluding swine) (specify) ;
Swine Birds (specify) ;
Rabbits Other leporidae (specify) ;
Wild game: Cloven hoofed (excluding swine) (specify) ;
Swine Birds (specify) ;
Soliped Leporidae (specify) ;
Others (specify) ;
8.2. Description of the meat products:
8.3. Nature of the pieces:
8.4. Nature of the packaging:
8.5. Number of pieces or packages:
8.6. Required storage and transport temperature:
8.7. Storage life:
8.8. Net weight:

9. Animal health attestation I, the undersigned official veterinarian, certify that:
9.1. The meat product contains the following meat constituents and meets the criteria indicated below:
Species (A)
Treatment (B)
Origin (C) (A) Insert the code for the relevant species of meat where BOV = domestic bovine animals (Bos Taurus, Bison bison, Bubalus bubalus and their crossbreds); OVI = domestic sheep (Ovis aries) and goats (Capra hircus); EQI = domestic equine animals (Equus caballus, Equus asinus and their crossbreds), POR = domestic porcine animals (Sus scrofa); RAB = domestic rabbits, PFG = domestic poultry and farmed feathered game, RUF farmed non-domestic animals other than suidae and solipeds; RUW = wild non-domestic animals other than suidae and solipeds; SUW = wild non-domestic suidae: EQW = wild non-domestic solipeds, WLP = wild leporidae, WGB = wild game birds.
(B) Insert A, B, C, D, E or F for the required treatment as specified and defined in Parts 2, 3 and 4 of Annex II to Commission Decision 2005/432/EC.
(C) Insert the ISO code of the country of origin and, in the case of regionalisation by Community legislation for the relevant meat constituents, the region as indicated in Part 1 of Annex II to Decision 2005/432/EC.
(5) 9.2. The meat product described in 9.1 has been prepared from fresh meat from bovine, ovine, caprine, porcine, soliped, farmed and wild game animals from these species and the fresh meat used in the production of the meat products:
either [9.2.1. has undergone a non-specific treatment as specified and defined under point A in Part 4 of Annex II to Decision 2005/432/EC and:] (5) either [9.2.1.1. satisfies the animal and public health requirements laid down in the appropriate health certificate(s) in Annex II Part 2 of Council Decision 79/542/EEC, and originates from a third country, or part thereof in the case of regionalization by Community legislation, as described in the relevant column of part 2 of Annex II of Decision 2005/432/EC;] (5) or [9.2.1.1. originates in a Member State of the European Community;] (5) or [9.2.1. meets any requirements agreed under the provisions of Directive 2002/99/EC and has undergone the specific treatment laid down for the third country of origin or part thereof for the meat of the species concerned in Parts 2 or 3 (as appropriate) of Annex II to Decision 2005/432/EC.] (5) (5) 9.3. The meat product described in 9.1 has been prepared from fresh meat from domestic poultry that:
either [9.3.1. has undergone a non-specific treatment as specified and defined under Part 4(A) of Annex II to Decision 2005/432/EC] and: (5) either [9.3.1.1. satisfies the animal health requirements laid down in Commission Decisions 94/984/EC], (5) or [9.3.1.1. originates in a Member State of the European Community satisfying the requirements of Articles 3, 4 and 5 of Council Directive 91/494/EEC] (5) either [9.3.1. originates in a third country referred to in Annex II, Chapter I, to Council Directive 92/118/EEC and has undergone the specific treatment laid down for the third country of origin or part thereof for the meat of the species concerned in Parts 2 or 3 (as appropriate) of Annex II to Decision 2005/432/EC] (5) (5) [9.4. in the case of meat products derived from fresh meat from leporidae and other land mammals:
satisfies the relevant animal health and public health requirements laid down in Commission Decision 2000/585/EC;]
9.5. the meat product:
9.5.1. [consists of meat and/or meat products derived from a single species, and has undergone the treatment satisfying the relevant conditions laid down in Annex II to Decision 2005/432/EC]
or (5) 9.5.1. [consists of meat from more than one species where, after mixing the meats together, the entire product has subsequently undergone a treatment which was at least equal to the most severe treatment required for any of the individual meat components contained in the meat product, as laid down in Annex II to Decision 2005/432/EC,]
or (5) 9.5.1. [has been prepared from meat, from more than one species where each of the constituent meats had previously undergone a treatment prior to mixing which satisfied the relevant treatment requirements for meat from that species, as laid down in Annex II to Decision 2005/432/EC]; (5)

9.6. after treatment all precautions to avoid contamination have been taken.
(5) [9.7. Additional guarantees:
in the case of poultry meat products which have not undergone a specific treatment and are destined for Member States or regions thereof which have been recognised in accordance with Article 12 of Council Directive 90/539/EEC, the poultry meat was derived from poultry which had not been vaccinated with a live vaccine against Newcastle disease within 30 days prior to slaughter;] 10. (5) (9) Public Health Attestation 10.1. the label affixed on the packaging of meat products described above, bear(s) a mark to the effect that the meat products come wholly from fresh meat from animals slaughtered in slaughterhouses approved for exporting to the European Community or, from animals slaughtered in a slaughterhouse specially for the delivery of meat for the required treatment as laid down in Part 2 and 3 of Annex II of Decision 2005/432/EC;
10.2. the meat products have as such been passed as fit for human consumption following a veterinary inspection carried out in accordance with the requirements of Council Directive 72/462/EEC;
10.3. the meat products have been obtained from pig meat which [has][has not] been subject to an examination for trichinosis and in the latter case has undergone cold treatment;
10.4. the means of transport and the loading conditions of meat products of this consignment meet the hygiene requirements laid down in respect of export to the European Community;
10.5. the meat products have been obtained from meat which satisfies the requirement of Chapter III of Directive 72/462/EEC and those of Article 3 to Council Directive 77/99/EEC, or have been obtained under the derogation provided for in Article 21a (2) of Directive 72/462/EEC. 11. (5) (10) I have read and understood Annex II, Chapter I of Directive 92/118/EEC (as last amended), including the specific provisions in that Chapter applying to the meat products described in 9.1 and certify that the products described in 9.1 meet the requirements provided for in that Chapter. 12. Official stamp and signature
Done at on
(Signature of official veterinarian)
(Stamp) (8) (Name in capital letters, qualifications and title)
Notes (1) Meat products as laid down in Article 2 (a) of Council Directive 77/99/EEC.
(2) Issued by the competent authority.
(3) Country and description of territory as appearing in Annex II to Decision 2005/432/EC.
(4) The registration number(s) of rail-wagon or lorry and the name of the ship should be given as appropriate. If known, the flight number of the aircraft.
(5) Keep as appropriate.
(6) Complete as appropriate.
(7) Mark box accordingly
(8) The colour of the signature shall be different to that of the printing. The same rule applies to the stamp other than those embossed or watermarked.
(9) In the case of meat products containing meat of bovine, ovine, caprine, porcine, soliped, farmed and wild game animals from these species.
(10) In the case of meat products containing meat of farmed and wild game birds, rabbit and wild leporidae.

(*1) Without prejudice to specific certification requirements provided for by Community agreements with third countries.

ANNEX IVTransit and/or storage

Model ‘TRANSIT/STORAGE’
1. Consignor (name and address in full)
VETERINARY CERTIFICATE
for meat product (1), for [transit]/[storage]( (2) (8) in the European Community No (3) ORIGINAL 3. Origin of the meat product (4) 2. Consignee (name and address in full)
3.1. Country:
3.2. Code of territory: 4. Competent Authority
4.1. Ministry:
4.2. Service: 5. Intended [transit]/[storage] (8) destination of the meat product
5.1. Storage in:
4.3. Local/regional level:
EU Member State:
Name and address of the establishment (6) (10): 6. Place of loading for exportation
5.2. Transit final third country destination (10):
Exit Community BIP name and address (10): 7. Means of transport and consignment identification (7) 7.3. Consignment identification details (9):
7.1. [Lorry]/[Rail-wagon]/[Ship]/[Aircraft] (8) 7.2. Registration number(s), ship name or flight number: 8. Identification of the meat product
8.1. Meat from: (animal species)
8.2. Temperature or other treatment applied to the meat product: (5) 8.3. Individual identification of the meat product included in this consignment:
Nature (9) Name and address of the establishment(s) Number of packages/pieces
Net weight (kg)
Total

9. Animal Health attestation
I, the undersigned official veterinarian, hereby certify, that the meat product described above:
9.1. comes from a country or region authorised for imports into the EC as laid down in Annex II to Decision 2005/432/EC at the time of slaughter of the animals from which the meat in the meat product is derived and
9.2. complies with the relevant animal health conditions as laid down in the animal health attestation in the model certificate in Annex III to Decision 2005/432/EC 10. Official stamp and signature
Done at on
(Signature of official veterinarian) (11) (Stamp) (11) (Name in capital letters, qualifications and title)
Notes
(1) Meat products as laid down in Article 2 (a) of Council Directive 77/99/EEC.
(2) In accordance with Articles 12(4) or 13 of Directive 97/78/EC.
(3) Issued by the competent authority.
(4) Country and description of territory as appearing in Annex II to Decision 2005/432/EC.
(5) Description of the treatment applied as laid down in Annex II to Decision 2005/432/EC.
(6) Address (and approval number if known) of the warehouse in a free zone, free warehouse, customs warehouse or ship chandler shall be included.
(7) The registration number(s) of rail-wagon or lorry and the name of the ship should be given as appropriate. If known, the flight number of the aircraft.
In case of transport in containers or boxes, the total number, their registration and seal numbers, if present, should be indicated under point 7.3. (8) Keep as appropriate.
(9) Complete if appropriate.
(10) Complete as appropriate.
(11) The colour of the signature shall be different to that of the printing. The same rule applies to the stamp other than those embossed or watermarked.

Pending: 32005D0343

4.5.2005 EN Official Journal of the European Union L 115/35
(1) Pursuant to Regulation (EC) No 1980/2000, the Community eco-label may be awarded to a product possessing characteristics which enable it to contribute significantly to improvements in relation to key environmental aspects.
(2) Regulation (EC) No 1980/2000 provides that specific eco-label criteria, drawn up on the basis of the criteria drafted by the European Union Eco-Labelling Board, are to be established according to product groups.
(3) It also provides that the review of eco-label criteria, as well as of the assessment and verification requirements related to those criteria, is to take place in good time before the end of the period of validity of the criteria specified for the product group concerned.
(4) It is appropriate, in order to reflect developments on the market, to revise the ecological criteria established by Commission Decision 2001/687/EC of 28 August 2001 establishing ecological criteria for the award of the Community eco‐label to portable computers(2).
(5) Furthermore, in order to specify that devices equipped with a touch screen keyboard are to be included in the product group and that products whose primary use is not computing are to be excluded, it is necessary to modify the definition of the product group laid down in that Decision.
(6) In the interests of clarity, Decision 2001/687/EC should therefore be replaced.
(7) The revised ecological criteria, and the related assessment and verification requirements, should be valid for a period of four years.
(8) It is appropriate to allow a transitional period of not more than 12 months for producers whose products have been awarded the eco-label before
(9)(10) the date of notification of this Decision or who have applied for such an award before that date, so that they have sufficient time to adapt their products to comply with the revised criteria and requirements.The measures provided for in this Decision are in accordance with the opinion of the Committee instituted by Article 17 of Regulation (EC) No 1980/2000,
— modem,
— network connection,
— keyboard or mouse action.
— the computer shall be designed so that the memory is easily accessible and can be changed,
— the computer shall be designed so that the hard disk, and if available either the CD drive or DVD drive, can be changed.
— 3,5 B(A) in the idle operating mode (equivalent to 35 dB(A)),
— 4,0 B(A) when accessing a hard-disk drive (equivalent to 40 dB(A)).
(a) one qualified person alone, shall be able to dismantle it;
(b) the manufacturer shall check the disassembly of the unit and provide a disassembly report that shall be made available to third parties on request. Amongst others, the report shall confirm that:—connections are easy to find and accessible,—connections are as standardised as possible,—connections are accessible with commonly available tools,—the background lighting lamps of LCD monitors are easily separable; — connections are easy to find and accessible, — connections are as standardised as possible, — connections are accessible with commonly available tools, — the background lighting lamps of LCD monitors are easily separable;
— connections are easy to find and accessible,
— connections are as standardised as possible,
— connections are accessible with commonly available tools,
— the background lighting lamps of LCD monitors are easily separable;
— connections are easy to find and accessible,
— connections are as standardised as possible,
— connections are accessible with commonly available tools,
— the background lighting lamps of LCD monitors are easily separable;
(c) hazardous materials shall be separable;
(d) 90 % (by weight) of plastic and metal materials in the housing and chassis shall be technically recyclable;
(e) if labels are required, they shall be easily separable or inherent;
(f) plastic parts shall:—have no lead or cadmium intentionally added,—be of one polymer or compatible polymers, except for the cover, which shall consist of no more than two types of polymers which are separable,—contain no metal inlays that cannot be separated by a single person using simple tools; — have no lead or cadmium intentionally added, — be of one polymer or compatible polymers, except for the cover, which shall consist of no more than two types of polymers which are separable, — contain no metal inlays that cannot be separated by a single person using simple tools;
— have no lead or cadmium intentionally added,
— be of one polymer or compatible polymers, except for the cover, which shall consist of no more than two types of polymers which are separable,
— contain no metal inlays that cannot be separated by a single person using simple tools;
— have no lead or cadmium intentionally added,
— be of one polymer or compatible polymers, except for the cover, which shall consist of no more than two types of polymers which are separable,
— contain no metal inlays that cannot be separated by a single person using simple tools;
(g) plastic parts shall not contain polybrominated biphenyl (PBB) or polybrominated diphenyl ether (PBDE) flame retardants as listed in Article 4 of Directive 2002/95/EC of the European Parliament and of the Council(3). This requirement shall take account of subsequent adaptations and amendments made to that Directive regarding the use of Deca-BDE.Plastic parts shall not contain chloroparaffin flame retardants with chain length 10 to 17 carbon atoms and chlorine content greater than 50 % by weight (CAS No 85535-84-8 and CAS No 85535-85-9).The applicant shall declare compliance with this requirement to the competent body;
(h) plastic parts heavier than 25 grams shall not contain flame retardant substances or preparations that are assigned at the time of applying for the eco-label any of the risk phrases:Dangerous for health:R45 (may cause cancer)R46 (may cause heritable genetic damage)R60 (may impair fertility)R61 (may cause harm to the unborn child)Dangerous for the environment:R50 (very toxic to aquatic organisms)R50/R53 (very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environmentR51/R53 (toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment)as defined in Council Directive 67/548/EEC(4); Dangerous for health:R45 (may cause cancer)R46 (may cause heritable genetic damage)R60 (may impair fertility)R61 (may cause harm to the unborn child) R45 (may cause cancer) R46 (may cause heritable genetic damage) R60 (may impair fertility) R61 (may cause harm to the unborn child) Dangerous for the environment:R50 (very toxic to aquatic organisms)R50/R53 (very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environmentR51/R53 (toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment)as defined in Council Directive 67/548/EEC(4); R50 (very toxic to aquatic organisms) R50/R53 (very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment R51/R53 (toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment) as defined in Council Directive 67/548/EEC(4);
Dangerous for health:R45 (may cause cancer)R46 (may cause heritable genetic damage)R60 (may impair fertility)R61 (may cause harm to the unborn child) R45 (may cause cancer) R46 (may cause heritable genetic damage) R60 (may impair fertility) R61 (may cause harm to the unborn child)
R45 (may cause cancer)
R46 (may cause heritable genetic damage)
R60 (may impair fertility)
R61 (may cause harm to the unborn child)
Dangerous for the environment:R50 (very toxic to aquatic organisms)R50/R53 (very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environmentR51/R53 (toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment)as defined in Council Directive 67/548/EEC(4); R50 (very toxic to aquatic organisms) R50/R53 (very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment R51/R53 (toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment) as defined in Council Directive 67/548/EEC(4);
R50 (very toxic to aquatic organisms)
R50/R53 (very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment
R51/R53 (toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment)
as defined in Council Directive 67/548/EEC(4);
Dangerous for health:R45 (may cause cancer)R46 (may cause heritable genetic damage)R60 (may impair fertility)R61 (may cause harm to the unborn child) R45 (may cause cancer) R46 (may cause heritable genetic damage) R60 (may impair fertility) R61 (may cause harm to the unborn child)
R45 (may cause cancer)
R46 (may cause heritable genetic damage)
R60 (may impair fertility)
R61 (may cause harm to the unborn child)
R45 (may cause cancer)
R46 (may cause heritable genetic damage)
R60 (may impair fertility)
R61 (may cause harm to the unborn child)
Dangerous for the environment:R50 (very toxic to aquatic organisms)R50/R53 (very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environmentR51/R53 (toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment)as defined in Council Directive 67/548/EEC(4); R50 (very toxic to aquatic organisms) R50/R53 (very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment R51/R53 (toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment) as defined in Council Directive 67/548/EEC(4);
R50 (very toxic to aquatic organisms)
R50/R53 (very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment
R51/R53 (toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment)
as defined in Council Directive 67/548/EEC(4);
R50 (very toxic to aquatic organisms)
R50/R53 (very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment
R51/R53 (toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment)
as defined in Council Directive 67/548/EEC(4);
(i) plastic parts shall have a permanent marking identifying the material, in conformity with ISO 11469:2000. Excluded from this criterion are extruded plastic materials and the light-guide of flat panel displays;
(j) batteries shall not contain more than 0,0001 % of mercury, 0,001 % of cadmium or 0,01 % of lead by weight of the battery.
(a) recommendations for the use of the power management features, including information that disabling these features can lead to higher consumption of energy and thus can increase the running costs;
(b) information that the energy drawn from the mains can be reduced to zero if the power supply is unplugged or if the wall socket is switched off;
(c) information on the guarantee and the availability of spare parts. When it is appropriate for the consumer to upgrade or exchange components, information on the proper procedures shall be given;
(d) information about the fact that the product has been designed to enable proper reuse of parts and recycling and should not be thrown away;
(e) advice on how the consumer can make use of the manufacturer's take-back offer;
(f) information as to how to make appropriate use of wireless local area network (WLAN) cards thus minimising security risks;
(g) information that the product has been awarded the Community eco-label with a brief explanation as to what this means together with an indication that more information on the eco-label can be found at the website address (http://europa.eu.int/ecolabel).
(a) All packaging components shall be easily separable by hand into individual materials to facilitate recycling.
(b) Where used, cardboard packaging shall consist of at least 80 % recycled material.
— reduced energy consumption,
— designed to facilitate recycling,
— reduced noise level.
THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Regulation (EC) No 1980/2000 of the European Parliament and of the Council of 17 July 2000 on a revised Community eco-label award scheme(1), and in particular the second subparagraph of Article 6(1) thereof,
After consulting the European Union Eco-Labelling Board,
(1) Pursuant to Regulation (EC) No 1980/2000, the Community eco-label may be awarded to a product possessing characteristics which enable it to contribute significantly to improvements in relation to key environmental aspects.
(2) Regulation (EC) No 1980/2000 provides that specific eco-label criteria, drawn up on the basis of the criteria drafted by the European Union Eco-Labelling Board, are to be established according to product groups.
(3) It also provides that the review of eco-label criteria, as well as of the assessment and verification requirements related to those criteria, is to take place in good time before the end of the period of validity of the criteria specified for the product group concerned.
(4) It is appropriate, in order to reflect developments on the market, to revise the ecological criteria established by Commission Decision 2001/687/EC of 28 August 2001 establishing ecological criteria for the award of the Community eco‐label to portable computers(2).
(5) Furthermore, in order to specify that devices equipped with a touch screen keyboard are to be included in the product group and that products whose primary use is not computing are to be excluded, it is necessary to modify the definition of the product group laid down in that Decision.
(6) In the interests of clarity, Decision 2001/687/EC should therefore be replaced.
(7) The revised ecological criteria, and the related assessment and verification requirements, should be valid for a period of four years.
(8) It is appropriate to allow a transitional period of not more than 12 months for producers whose products have been awarded the eco-label before
(9)(10) the date of notification of this Decision or who have applied for such an award before that date, so that they have sufficient time to adapt their products to comply with the revised criteria and requirements.The measures provided for in this Decision are in accordance with the opinion of the Committee instituted by Article 17 of Regulation (EC) No 1980/2000,
HAS ADOPTED THIS DECISION:

Article 1
The product group ‘portable computers’ shall comprise all computers which can be used in multiple locations, which consist of a system unit, display and keyboard combined in a single case, which are intended to be easily transported between locations and which can be used with an internal battery.
That product group shall also cover devices equipped with a touch screen keyboard.
The product group shall not cover products whose primary use is not computing.

Article 2
In order to be awarded the Community eco-label, for portable computers, under Regulation (EC) No 1980/2000, an appliance must fall within the product group ‘portable computers’ and must comply with the ecological criteria set out in the Annex to this Decision.

Article 3
The ecological criteria for the product group ‘portable computers’, as well as the related assessment and verification requirements, shall be valid until 30 April 2009.

Article 4
For administrative purposes, the code number assigned to the product group ‘portable computers’ shall be ‘018’.

Article 5
Decision 2001/687/EC is repealed.

Article 6
Eco-labels awarded before the date of notification of this Decision in respect of products falling within the product group ‘portable computers’ may continue to be used until 31 March 2006.
Where applications have been submitted before the date of notification of this Decision for award of the eco-label in respect of products falling within the product group ‘portable computers’, those products may be awarded the eco-label under the conditions laid down in Decision 2001/687/EC. In such cases the eco-label may be used until 31 March 2006.

Article 7
This Decision is addressed to the Member States.

THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Regulation (EC) No 1980/2000 of the European Parliament and of the Council of 17 July 2000 on a revised Community eco-label award scheme(1), and in particular the second subparagraph of Article 6(1) thereof,
After consulting the European Union Eco-Labelling Board,
(1) Pursuant to Regulation (EC) No 1980/2000, the Community eco-label may be awarded to a product possessing characteristics which enable it to contribute significantly to improvements in relation to key environmental aspects.
(2) Regulation (EC) No 1980/2000 provides that specific eco-label criteria, drawn up on the basis of the criteria drafted by the European Union Eco-Labelling Board, are to be established according to product groups.
(3) It also provides that the review of eco-label criteria, as well as of the assessment and verification requirements related to those criteria, is to take place in good time before the end of the period of validity of the criteria specified for the product group concerned.
(4) It is appropriate, in order to reflect developments on the market, to revise the ecological criteria established by Commission Decision 2001/687/EC of 28 August 2001 establishing ecological criteria for the award of the Community eco‐label to portable computers(2).
(5) Furthermore, in order to specify that devices equipped with a touch screen keyboard are to be included in the product group and that products whose primary use is not computing are to be excluded, it is necessary to modify the definition of the product group laid down in that Decision.
(6) In the interests of clarity, Decision 2001/687/EC should therefore be replaced.
(7) The revised ecological criteria, and the related assessment and verification requirements, should be valid for a period of four years.
(8) It is appropriate to allow a transitional period of not more than 12 months for producers whose products have been awarded the eco-label before
(9)(10) the date of notification of this Decision or who have applied for such an award before that date, so that they have sufficient time to adapt their products to comply with the revised criteria and requirements.The measures provided for in this Decision are in accordance with the opinion of the Committee instituted by Article 17 of Regulation (EC) No 1980/2000,
HAS ADOPTED THIS DECISION:
The product group ‘portable computers’ shall comprise all computers which can be used in multiple locations, which consist of a system unit, display and keyboard combined in a single case, which are intended to be easily transported between locations and which can be used with an internal battery.
That product group shall also cover devices equipped with a touch screen keyboard.
The product group shall not cover products whose primary use is not computing.
In order to be awarded the Community eco-label, for portable computers, under Regulation (EC) No 1980/2000, an appliance must fall within the product group ‘portable computers’ and must comply with the ecological criteria set out in the Annex to this Decision.
The ecological criteria for the product group ‘portable computers’, as well as the related assessment and verification requirements, shall be valid until 30 April 2009.
For administrative purposes, the code number assigned to the product group ‘portable computers’ shall be ‘018’.
Decision 2001/687/EC is repealed.
Eco-labels awarded before the date of notification of this Decision in respect of products falling within the product group ‘portable computers’ may continue to be used until 31 March 2006.
Where applications have been submitted before the date of notification of this Decision for award of the eco-label in respect of products falling within the product group ‘portable computers’, those products may be awarded the eco-label under the conditions laid down in Decision 2001/687/EC. In such cases the eco-label may be used until 31 March 2006.
This Decision is addressed to the Member States.

ECOLOGICAL CRITERIA

ANNEXFRAMEWORKIn order to qualify for the eco-label, a portable computer (hereinafter referred to as ‘the product’) must fall within the product group as defined in Article 1, and must comply with the following criteria in this Annex and with tests carried out on application as indicated in the criteria. Testing shall be performed by laboratories that meet the general requirements expressed in standard EN ISO 17025. Where appropriate, other test methods may be used if their equivalence is accepted by the competent body assessing the application. Where no tests are mentioned, or are mentioned as being for use in verification or monitoring, competent bodies should rely, as appropriate, on declarations and documentation provided by the applicant and/or independent verifications.
The competent bodies are recommended to take into account the implementation of recognised environmental management schemes, such as EMAS or ISO 14001, when assessing applications and monitoring compliance with the criteria in this Annex. (Note:it is not required to implement such management schemes.)
1. Energy savingsThe portable computer shall be equipped with an easily accessible on/off switch.
The portable computer shall support the ACPI(1)S3 sleep state (suspend to RAM) to allow minimum energy consumption of no more than 3 watts. The computer shall be able to wake up from this mode in response to a command from any of the following:

— | modem,
— | network connection,
— | keyboard or mouse action.The default mode-change time from operation to the ACPI S3 sleep state shall be no more than 15 minutes of inactivity. The manufacturer must enable this feature.
The portable computer shall have a maximum off-mode consumption of no more than 2 watts when the battery is fully charged and the power supply is connected to the electricity supply. In this context, the off-mode is the state initiated through the command to shut down the computer.
The power supply of the portable computer shall have a maximum consumption of no more than 0,75 watt when it is connected to the electricity supply but is not connected to the computer.
The applicant shall provide the competent body with a report certifying that the level of power consumption in both the ACPI S3 mode and the off-mode have been measured using the procedure in the current Energy Star(2)computer memorandum of understanding. The report shall state the measured power consumptions in both of these modes. The applicant shall declare compliance with the power supply requirement.
2. Lifetime extensionThe availability of compatible batteries and power supplies and of the keyboard and its parts shall be guaranteed for three years from the time that production ceases. In addition the portable computer shall meet the following criteria:

— | the computer shall be designed so that the memory is easily accessible and can be changed,
— | the computer shall be designed so that the hard disk, and if available either the CD drive or DVD drive, can be changed.The applicant shall declare the compliance of the product with these requirements to the competent body.
3. Mercury content of the displayThe background lighting of the flat panel display shall not contain more than 3 mg of mercury on average per lamp. The display of a personal data assistant (PDA) shall contain no mercury.
The applicant shall declare the compliance of the product with these requirements to the competent body.
4. NoiseThe ‘declared A-weighted sound power level’ (re lpW) of the portable computer, according to paragraph 3.2.5 of ISO 9296, shall not exceed:

— | 3,5 B(A) in the idle operating mode (equivalent to 35 dB(A)),
— | 4,0 B(A) when accessing a hard-disk drive (equivalent to 40 dB(A)).The applicant shall provide a report to the competent body, prepared by an independent test laboratory accredited to ISO 17025, certifying that the levels of noise emissions have been measured in accordance with ISO 7779 and declared in accordance with ISO 9296. The report shall state the measured levels of noise emissions in both the idle operating mode and when accessing a disk drive, and be declared in accordance with paragraph 3.2.5 of ISO 9296.
5. Electromagnetic emissionsThe portable computer shall meet the requirements set out in EN50279, Category A.
The applicant shall provide a report to the competent body showing that the product’s emissions are compliant with the requirement.
6. Take-back, recycling and hazardous substancesThe manufacturer shall offer, free-of-charge, the take-back for refurbishment or recycling of the product and for any component being replaced, except for items contaminated by users (e.g. in medical or nuclear applications). In addition, the product shall meet the following criteria:

(a) | one qualified person alone, shall be able to dismantle it;
(b) | the manufacturer shall check the disassembly of the unit and provide a disassembly report that shall be made available to third parties on request. Amongst others, the report shall confirm that:—connections are easy to find and accessible,—connections are as standardised as possible,—connections are accessible with commonly available tools,—the background lighting lamps of LCD monitors are easily separable; | — | connections are easy to find and accessible, | — | connections are as standardised as possible, | — | connections are accessible with commonly available tools, | — | the background lighting lamps of LCD monitors are easily separable;
— | connections are easy to find and accessible,
— | connections are as standardised as possible,
— | connections are accessible with commonly available tools,
— | the background lighting lamps of LCD monitors are easily separable;
(c) | hazardous materials shall be separable;
(d) | 90 % (by weight) of plastic and metal materials in the housing and chassis shall be technically recyclable;
(e) | if labels are required, they shall be easily separable or inherent;
(f) | plastic parts shall:—have no lead or cadmium intentionally added,—be of one polymer or compatible polymers, except for the cover, which shall consist of no more than two types of polymers which are separable,—contain no metal inlays that cannot be separated by a single person using simple tools; | — | have no lead or cadmium intentionally added, | — | be of one polymer or compatible polymers, except for the cover, which shall consist of no more than two types of polymers which are separable, | — | contain no metal inlays that cannot be separated by a single person using simple tools;
— | have no lead or cadmium intentionally added,
— | be of one polymer or compatible polymers, except for the cover, which shall consist of no more than two types of polymers which are separable,
— | contain no metal inlays that cannot be separated by a single person using simple tools;
(g) | plastic parts shall not contain polybrominated biphenyl (PBB) or polybrominated diphenyl ether (PBDE) flame retardants as listed in Article 4 of Directive 2002/95/EC of the European Parliament and of the Council(3). This requirement shall take account of subsequent adaptations and amendments made to that Directive regarding the use of Deca-BDE.Plastic parts shall not contain chloroparaffin flame retardants with chain length 10 to 17 carbon atoms and chlorine content greater than 50 % by weight (CAS No 85535-84-8 and CAS No 85535-85-9).The applicant shall declare compliance with this requirement to the competent body;
(h) | plastic parts heavier than 25 grams shall not contain flame retardant substances or preparations that are assigned at the time of applying for the eco-label any of the risk phrases:Dangerous for health:R45 (may cause cancer)R46 (may cause heritable genetic damage)R60 (may impair fertility)R61 (may cause harm to the unborn child)Dangerous for the environment:R50 (very toxic to aquatic organisms)R50/R53 (very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environmentR51/R53 (toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment)as defined in Council Directive 67/548/EEC(4); | | Dangerous for health:R45 (may cause cancer)R46 (may cause heritable genetic damage)R60 (may impair fertility)R61 (may cause harm to the unborn child) | | R45 (may cause cancer) | | R46 (may cause heritable genetic damage) | | R60 (may impair fertility) | | R61 (may cause harm to the unborn child) | | Dangerous for the environment:R50 (very toxic to aquatic organisms)R50/R53 (very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environmentR51/R53 (toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment)as defined in Council Directive 67/548/EEC(4); | | R50 (very toxic to aquatic organisms) | | R50/R53 (very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment | | R51/R53 (toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment) | | as defined in Council Directive 67/548/EEC(4);
| Dangerous for health:R45 (may cause cancer)R46 (may cause heritable genetic damage)R60 (may impair fertility)R61 (may cause harm to the unborn child) | | R45 (may cause cancer) | | R46 (may cause heritable genetic damage) | | R60 (may impair fertility) | | R61 (may cause harm to the unborn child)
| R45 (may cause cancer)
| R46 (may cause heritable genetic damage)
| R60 (may impair fertility)
| R61 (may cause harm to the unborn child)
| Dangerous for the environment:R50 (very toxic to aquatic organisms)R50/R53 (very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environmentR51/R53 (toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment)as defined in Council Directive 67/548/EEC(4); | | R50 (very toxic to aquatic organisms) | | R50/R53 (very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment | | R51/R53 (toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment) | | as defined in Council Directive 67/548/EEC(4);
| R50 (very toxic to aquatic organisms)
| R50/R53 (very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment
| R51/R53 (toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment)
| as defined in Council Directive 67/548/EEC(4);
(i) | plastic parts shall have a permanent marking identifying the material, in conformity with ISO 11469:2000. Excluded from this criterion are extruded plastic materials and the light-guide of flat panel displays;
(j) | batteries shall not contain more than 0,0001 % of mercury, 0,001 % of cadmium or 0,01 % of lead by weight of the battery.The applicant shall declare the compliance of the product with these requirements and shall provide to the competent body assessing the application a copy of the disassembly report.
With reference to criterion 6(h), the flame retardants that are used, if any, shall not have been assigned any of the above risk phrases nor shall they be named in Annex 1 to Directive 67/548/EEC or its subsequent amendments regarding the classification, packaging and labelling of dangerous substances. This requirement does not apply to flame retardants that on application change their chemical nature to no longer warrant classification under any of the R-phrases listed above, and where less than 0,1 % of the flame retardant in the treated part remains in the form as before application. Any flame retardants that are used in plastic parts >25g must be specified in the application documentation by giving their name and CAS number.
7. User instructionsThe product shall be sold with relevant user information, which provides advice on proper environmental use and, in particular:

(a) | recommendations for the use of the power management features, including information that disabling these features can lead to higher consumption of energy and thus can increase the running costs;
(b) | information that the energy drawn from the mains can be reduced to zero if the power supply is unplugged or if the wall socket is switched off;
(c) | information on the guarantee and the availability of spare parts. When it is appropriate for the consumer to upgrade or exchange components, information on the proper procedures shall be given;
(d) | information about the fact that the product has been designed to enable proper reuse of parts and recycling and should not be thrown away;
(e) | advice on how the consumer can make use of the manufacturer’s take-back offer;
(f) | information as to how to make appropriate use of wireless local area network (WLAN) cards thus minimising security risks;
(g) | information that the product has been awarded the Community eco-label with a brief explanation as to what this means together with an indication that more information on the eco-label can be found at the website address (http://europa.eu.int/ecolabel).The applicant shall declare the compliance of the product with these requirements, and shall provide a copy of the instruction manual to the competent body assessing the application.
8. PackagingPackaging shall meet the following requirements:

(a) | All packaging components shall be easily separable by hand into individual materials to facilitate recycling.
(b) | Where used, cardboard packaging shall consist of at least 80 % recycled material.Assessment and verification: The applicant shall declare compliance with the requirement and provide a sample(s) of the packaging to the awarding competent body as part of the application.
9. Information appearing on the eco-labelBox 2 of the eco-label shall include the following text:

— | reduced energy consumption,
— | designed to facilitate recycling,
— | reduced noise level.The applicant shall declare the compliance of the product with this requirement, and shall provide a copy of the eco-label as it will appear on the packaging and/or product and/or accompanying documentation to the competent body.

(1) Advanced configuration and power interface (ACPI).
(2) As defined by the United States Environmental Protection Agency, http://www.energystar.gov/index.cfm?c=computers.pr_crit_computers
(3)
OJ L 37,13.2.2003, p. 19.
(4)
OJ L 196, 16.8.1967, p. 1.

Pending: 32005D0342

4.5.2005 EN Official Journal of the European Union L 115/9
(1) Under Regulation (EC) No 1980/2000 the Community eco-label may be awarded to a product possessing characteristics which enable it to contribute significantly to improvements in relation to key environmental aspects.
(2) Regulation (EC) No 1980/2000 provides that specific eco-label criteria, drawn up on the basis of the criteria drafted by the European Union Eco-Labelling Board, are to be established according to product groups.
(3) It also provides that the review of the eco-label criteria, as well as of the assessment and verification requirements related to the criteria, is to take place in good time before the end of the period of validity of the criteria specified for the product group concerned.
(4) It is appropriate, in order to take account of scientific and market developments, to revise the ecological criteria established by Commission Decision 2001/607/EC of 19 July 2001 establishing the ecological criteria for the award of the Community eco-label to hand dishwashing detergents ((2)).
(5) Furthermore, in order to specify that products for both private and professional use are covered, it is necessary to modify the definition of the product group laid down in that Decision.
(6) In the interests of clarity, Decision 2001/607/EC should therefore be replaced.
(7) The revised ecological criteria should be valid for a period of four years.
(8) It is appropriate to allow a transitional period of not more than 12 months for applicants whose products have been awarded the eco-label before the date of notification of this Decision or who have applied for such an award before that date, so that they have sufficient time to adapt their products to comply with the revised criteria and requirements.
(9) The measures provided for in this Decision are in accordance with the opinion of the Committee instituted by Article 17 of Regulation (EC) No 1980/2000,
— the reduction of discharges of toxic or otherwise polluting substances into the aquatic environment,
— the reduction or prevention of risks to health or the environment related to the use of hazardous substances,
— the minimisation of packaging waste,
— information that will enable the consumer to use the product in the way that is efficient and minimises environmental impact.
(a) The following ingredients shall not be included in the product, either as part of the formulation or as part of any preparation included in the formulation:—alkyl phenol ethoxylates (APEOs) and derivatives thereof—EDTA (ethylene-diamine-tetra-acetic acid) and its salts—NTA (nitrilo-tri-acetate)—nitromusks and polycyclic musks, including for example:—musk xylene: 5-tert-butyl-2,4,6-trinitro-m-xylene—musk ambrette: 4-tert-butyl-3-methoxy-2,6-dinitrotoluene—moskene: 1,1,3,3,5-pentamethyl-4,6-dinitroindan—musk tibetine: 1-tert-butyl-3,4,5-trimethyl-2,6-dinitrobenzene—musk ketone: 4'-tert-butyl-2',6'-dimethyl-3',5'-dinitroacetaphenone—HHCB (1,3,4,6,7,8-Hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran)—AHTN (6-Acetyl-1,1,2,4,4,7-hexamethyltetralin).Assessment and verification: the applicant shall provide a declaration supported by declarations from manufacturers, as appropriate, confirming that the listed substances have not been included in the product. — alkyl phenol ethoxylates (APEOs) and derivatives thereof — EDTA (ethylene-diamine-tetra-acetic acid) and its salts — NTA (nitrilo-tri-acetate) — nitromusks and polycyclic musks, including for example:—musk xylene: 5-tert-butyl-2,4,6-trinitro-m-xylene—musk ambrette: 4-tert-butyl-3-methoxy-2,6-dinitrotoluene—moskene: 1,1,3,3,5-pentamethyl-4,6-dinitroindan—musk tibetine: 1-tert-butyl-3,4,5-trimethyl-2,6-dinitrobenzene—musk ketone: 4'-tert-butyl-2',6'-dimethyl-3',5'-dinitroacetaphenone—HHCB (1,3,4,6,7,8-Hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran)—AHTN (6-Acetyl-1,1,2,4,4,7-hexamethyltetralin). — musk xylene: 5-tert-butyl-2,4,6-trinitro-m-xylene — musk ambrette: 4-tert-butyl-3-methoxy-2,6-dinitrotoluene — moskene: 1,1,3,3,5-pentamethyl-4,6-dinitroindan — musk tibetine: 1-tert-butyl-3,4,5-trimethyl-2,6-dinitrobenzene — musk ketone: 4'-tert-butyl-2',6'-dimethyl-3',5'-dinitroacetaphenone — HHCB (1,3,4,6,7,8-Hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran) — AHTN (6-Acetyl-1,1,2,4,4,7-hexamethyltetralin).
— alkyl phenol ethoxylates (APEOs) and derivatives thereof
— EDTA (ethylene-diamine-tetra-acetic acid) and its salts
— NTA (nitrilo-tri-acetate)
— nitromusks and polycyclic musks, including for example:—musk xylene: 5-tert-butyl-2,4,6-trinitro-m-xylene—musk ambrette: 4-tert-butyl-3-methoxy-2,6-dinitrotoluene—moskene: 1,1,3,3,5-pentamethyl-4,6-dinitroindan—musk tibetine: 1-tert-butyl-3,4,5-trimethyl-2,6-dinitrobenzene—musk ketone: 4'-tert-butyl-2',6'-dimethyl-3',5'-dinitroacetaphenone—HHCB (1,3,4,6,7,8-Hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran)—AHTN (6-Acetyl-1,1,2,4,4,7-hexamethyltetralin). — musk xylene: 5-tert-butyl-2,4,6-trinitro-m-xylene — musk ambrette: 4-tert-butyl-3-methoxy-2,6-dinitrotoluene — moskene: 1,1,3,3,5-pentamethyl-4,6-dinitroindan — musk tibetine: 1-tert-butyl-3,4,5-trimethyl-2,6-dinitrobenzene — musk ketone: 4'-tert-butyl-2',6'-dimethyl-3',5'-dinitroacetaphenone — HHCB (1,3,4,6,7,8-Hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran) — AHTN (6-Acetyl-1,1,2,4,4,7-hexamethyltetralin).
— musk xylene: 5-tert-butyl-2,4,6-trinitro-m-xylene
— musk ambrette: 4-tert-butyl-3-methoxy-2,6-dinitrotoluene
— moskene: 1,1,3,3,5-pentamethyl-4,6-dinitroindan
— musk tibetine: 1-tert-butyl-3,4,5-trimethyl-2,6-dinitrobenzene
— musk ketone: 4'-tert-butyl-2',6'-dimethyl-3',5'-dinitroacetaphenone
— HHCB (1,3,4,6,7,8-Hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran)
— AHTN (6-Acetyl-1,1,2,4,4,7-hexamethyltetralin).
— alkyl phenol ethoxylates (APEOs) and derivatives thereof
— EDTA (ethylene-diamine-tetra-acetic acid) and its salts
— NTA (nitrilo-tri-acetate)
— nitromusks and polycyclic musks, including for example:—musk xylene: 5-tert-butyl-2,4,6-trinitro-m-xylene—musk ambrette: 4-tert-butyl-3-methoxy-2,6-dinitrotoluene—moskene: 1,1,3,3,5-pentamethyl-4,6-dinitroindan—musk tibetine: 1-tert-butyl-3,4,5-trimethyl-2,6-dinitrobenzene—musk ketone: 4'-tert-butyl-2',6'-dimethyl-3',5'-dinitroacetaphenone—HHCB (1,3,4,6,7,8-Hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran)—AHTN (6-Acetyl-1,1,2,4,4,7-hexamethyltetralin). — musk xylene: 5-tert-butyl-2,4,6-trinitro-m-xylene — musk ambrette: 4-tert-butyl-3-methoxy-2,6-dinitrotoluene — moskene: 1,1,3,3,5-pentamethyl-4,6-dinitroindan — musk tibetine: 1-tert-butyl-3,4,5-trimethyl-2,6-dinitrobenzene — musk ketone: 4'-tert-butyl-2',6'-dimethyl-3',5'-dinitroacetaphenone — HHCB (1,3,4,6,7,8-Hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran) — AHTN (6-Acetyl-1,1,2,4,4,7-hexamethyltetralin).
— musk xylene: 5-tert-butyl-2,4,6-trinitro-m-xylene
— musk ambrette: 4-tert-butyl-3-methoxy-2,6-dinitrotoluene
— moskene: 1,1,3,3,5-pentamethyl-4,6-dinitroindan
— musk tibetine: 1-tert-butyl-3,4,5-trimethyl-2,6-dinitrobenzene
— musk ketone: 4'-tert-butyl-2',6'-dimethyl-3',5'-dinitroacetaphenone
— HHCB (1,3,4,6,7,8-Hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran)
— AHTN (6-Acetyl-1,1,2,4,4,7-hexamethyltetralin).
— musk xylene: 5-tert-butyl-2,4,6-trinitro-m-xylene
— musk ambrette: 4-tert-butyl-3-methoxy-2,6-dinitrotoluene
— moskene: 1,1,3,3,5-pentamethyl-4,6-dinitroindan
— musk tibetine: 1-tert-butyl-3,4,5-trimethyl-2,6-dinitrobenzene
— musk ketone: 4'-tert-butyl-2',6'-dimethyl-3',5'-dinitroacetaphenone
— HHCB (1,3,4,6,7,8-Hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran)
— AHTN (6-Acetyl-1,1,2,4,4,7-hexamethyltetralin).
(b) Quaternary ammonium salts that are not readily biodegradable shall not be used, either as part of the formulation or as part of any preparation included in the formulation.Assessment and verification: the applicant shall provide documentation showing the biodegradability of any quaternary ammonium salt used.
(c) No ingredient (substance or preparation) shall be included in the product that is classified with any of the following risk phrases, or any combination thereof, in accordance with Council Directive 67/548/EEC of 27 June 1967 on the approximation of laws, regulations and administrative provisions relating to the classification, packaging and labelling of dangerous substances ((2)) and its amendments or Directive 1999/45/EC of the European Parliament and of the Council of 31 May 1999 concerning the approximation of the laws, regulations and administrative provisions of the Member States relating to the classification, packaging and labelling of dangerous preparations ((3)) and its amendments:R40 (limited evidence of a carcinogenic effect),R45 (may cause cancer),R46 (may cause heritable genetic damage),R49 (may cause cancer by inhalation),R68 (possible risks of irreversible effects),R50-53 (very toxic to aquatic organism and may cause long term adverse effects in the aquatic environment),R51-53 (toxic to aquatic organism and may cause long term adverse effects in the aquatic environment),R59 (dangerous to the ozone layer),R60 (may impair fertility),R61 (may cause harm to the unborn child),R62 (possible risk of impaired fertility),R63 (possible risk of harm to the unborn child),R64 (may cause harm to breastfed babies).Specific requirements are prescribed for biocides, either as part of the formulation or as part of any preparation included in the formulation (see criterion on biocides below).The above requirements shall apply to each ingredient (substance or preparation) that exceeds 0,01 % by weight of the final product. This includes also each ingredient of any preparation used in the formulation that exceeds 0,01 % by weight of the final product.Assessment and verification: copies of the material safety data sheets shall be provided for all ingredients (whether substances or preparations). A declaration prepared by the manufacturer of ingredients and showing compliance with this criterion shall be provided by the applicant. R40 (limited evidence of a carcinogenic effect), R45 (may cause cancer), R46 (may cause heritable genetic damage), R49 (may cause cancer by inhalation), R68 (possible risks of irreversible effects), R50-53 (very toxic to aquatic organism and may cause long term adverse effects in the aquatic environment), R51-53 (toxic to aquatic organism and may cause long term adverse effects in the aquatic environment), R59 (dangerous to the ozone layer), R60 (may impair fertility), R61 (may cause harm to the unborn child), R62 (possible risk of impaired fertility), R63 (possible risk of harm to the unborn child), R64 (may cause harm to breastfed babies).
R40 (limited evidence of a carcinogenic effect),
R45 (may cause cancer),
R46 (may cause heritable genetic damage),
R49 (may cause cancer by inhalation),
R68 (possible risks of irreversible effects),
R50-53 (very toxic to aquatic organism and may cause long term adverse effects in the aquatic environment),
R51-53 (toxic to aquatic organism and may cause long term adverse effects in the aquatic environment),
R59 (dangerous to the ozone layer),
R60 (may impair fertility),
R61 (may cause harm to the unborn child),
R62 (possible risk of impaired fertility),
R63 (possible risk of harm to the unborn child),
R64 (may cause harm to breastfed babies).
R40 (limited evidence of a carcinogenic effect),
R45 (may cause cancer),
R46 (may cause heritable genetic damage),
R49 (may cause cancer by inhalation),
R68 (possible risks of irreversible effects),
R50-53 (very toxic to aquatic organism and may cause long term adverse effects in the aquatic environment),
R51-53 (toxic to aquatic organism and may cause long term adverse effects in the aquatic environment),
R59 (dangerous to the ozone layer),
R60 (may impair fertility),
R61 (may cause harm to the unborn child),
R62 (possible risk of impaired fertility),
R63 (possible risk of harm to the unborn child),
R64 (may cause harm to breastfed babies).
(a) The product may only include biocides in order to preserve the product, and in the appropriate dosage for this purpose alone. This does not refer to surfactants, which may also have biocidal properties.Assessment and verification: copies of the material safety data sheets of any preservatives added shall be provided, together with information on their exact concentration in the final product. The manufacturer or supplier of the preservatives shall provide information on the dosage necessary to preserve the product.
(b) It is prohibited to claim or suggest on the packaging or by any other communication that the hand dishwashing product has an antimicrobial action.Assessment and verification: the texts and layouts used on each type of packaging and/or an example of each different type of packaging shall be provided to the competent body.
(c) Biocides, either as part of the formulation or as part of any preparation included in the formulation, that are used to preserve the product and that are classified with R50-53 or R51-53 risk phrases, in accordance with Directive 67/548/EEC and its amendments or Directive 1999/45/EC, are permitted but only if they are not potentially bioaccumulative. In this context, a biocide is considered to be potentially bioaccumulative if the log Pow(log octanol/water partition coefficient) ≥ 3,0 (unless the experimentally determined BCF ≤ 100).The concentration of biocides in the final product shall not exceed the maximum authorised concentration in Council Directive 76/768/EEC of 27 July 1976 on the approximation of the laws of the Member States relating to cosmetic products(4)and its subsequent amendments.Assessment and verification:copies of the material safety data sheets shall be provided for all biocides, together with a documentation of the concentrations of the biocides in the final product.
(a) The product shall not contain perfumes containing nitro-musks or polycyclic musks (as specified in the criterion 3a).
(b) Any ingredients added to the product as a fragrance must have been manufactured and/or handled in accordance with the code of practice of the International Fragrance Association.
(c) Fragrances shall not be used in hand dishwashing detergents for professional use.
(a) The primary packaging, except for the cap, shall have a volumetric coefficient of packaging (VCP) less than or equal to 1,9. This criterion does not apply if the primary packaging is made up of 50 % or more recycled material.VCP is equal to the volume of the smallest rectangular solid (rectangular parallelepiped) that can contain the packaging divided by the volume of the product contained in the packaging.
(b) If the primary packaging is made of recycled material, any indication of this on the packaging shall be in conformity with the ISO 14021 standard ‘Environmental labels and declarations — Self declared claims (type II environmental labelling)’.
(c) The primary packaging parts shall be easily separable into mono-material parts.
(d) Plastics that are used for the main container shall be marked according to European Parliament and Council Directive 94/62/EC of 20 December 1994 on packaging and packaging waste(6), or DIN 6120 part 1 and 2 in connection with DIN 7728 part 1.
(a) ‘To wash your dishes in the most efficient way, to save water and energy, and to protect the environment, do not use running water but immerse the dishes, and use the recommended dosage. You can wash most efficiently without lots of foam’ (or equivalent text);
(b) The information below shall appear on the packaging in a reasonably sufficient size and against a visible background. The use of pictograms is voluntary.Text of imageRecommended dosage for 5 litres of dishwashing water:not very dirty x ml (y tea spoons) of productdirty z ml (w tea spoons) of productwhere x, y, z and w have to be defined by the applicant and/or the manufacturer.The measure used in the above pictogram shall be millilitres. A second well-known metric, such as teaspoons, shall additionally be given in brackets (as in the pictogram above). However, if the packaging has an efficient and convenient dosing system that can provide an equally reliable dosage, an alternative metric (e.g. capfuls, squirts, or other) may be used;
(c) an indication of the approximate number of washes that the consumer can perform with one bottle is recommended but voluntary.This is calculated by dividing the volume of the product by the dosage required for 5 l of dishwashing detergent for dirty dishes (as indicated in the pictogram above);
(d) Regulation (EC) No 648/2004 shall be applied;
(e) ‘For more information visit the EU eco-label website: http://europa.eu.int/ecolabel’ (or equivalent text).
— reduced impact on aquatic life,
— reduced use of hazardous substances,
— clear user instructions.
Acute toxicity Chronic toxicity Degradation
DID No Ingredient name LC50/EC50 SF(acute) TF(acute) NOEC(*1) SF (chronic)(*1) TF (chronic) DF Aerobic Anaerobic
Anionic surfactants
1 Linear alkyl benzene sulphonates 11,5 – 11,8 (LAS) 4,1 1 000 0,0041 0,69 10 0,069 0,05 R N
2 LAS (C 10-13 alkyl) triethanolamine salt 4,2 1 000 0,0042 3,4 100 0,034 0,05 R O
3 C 14/17 Alkyl sulphonate 6,7 5 000 0,00134 0,44 10 0,044 0,05 R N
4 C 8/10 Alkyl sulphate 132 5 000 0,0264 0,0264 0,05 R Y
5 C 12/14 Alkyl sulphate (AS) 2,8 1 000 0,0028 2 100 0,02 0,05 R Y
6 C 12/18 Alkyl sulphate (AS)(1) 0,0149 0,027 0,05 R Y
7 C 16/18 Fatty alcohol sulphate (FAS) 27 1 000 0,027 1,7 50 0,034 0,05 R Y
8 C 12/15 A 1-3 EO sulphate 4,6 1 000 0,0046 0,1 10 0,01 0,05 R Y
9 C 16/18 A 3-4 EO sulphate 0,57 10 000 0,000057 0,000057 0,05 R Y
10 Dialkyl sulpho succinate 15,7 1 000 0,0157 0,0157 0,5 I N
11 C 12/14 Sulpho- fatty acid methylester 9 10 000 0,0009 0,23 50 0,0046 0,05 R N
12 C 16/18 Sulpho- fatty acid methylester 0,51 5 000 0,000102 0,2 50 0,004 0,05 R N
13 C 14/16 alfa Olefin sulphonate 3,3 10 000 0,00033 0,00033 0,05 R N
14 C 14/18 alfa Olefin sulphonate 0,5 5 000 0,0001 0,0001 0,05 R N
15 Soap C > 12-22 22 1 000 0,022 10 100 0,1 0,05 R Y
16 Lauroyl Sarcosinate 56 10 000 0,0056 0,0056 0,05 R Y
17 C 9/11 2-10 EO Carboxymethylated, sodium salt or acid 100 10 000 0,01 0,01 0,05 R O
18 C 12/18 2-10 EO Carboxymethylated, sodium salt or acid 8,8 1 000 0,0088 5 100 0,05 0,05 R O
19 C 12/18 Alkyl phosphate esters 38 1 000 0,038 0,038 0,05 R N
Non-ionic surfactants
20 C 8 A 1-5 EO 7,8 1 000 0,0078 0,0078 0,05 R Y
21 C 9/11 A, > 3-6 EO predominantly linear 5,6 1 000 0,0056 0,0056 0,05 R Y
22 C 9/11 A, > 6-10 EO predominantly linear 5 1 000 0,005 0,005 0,05 R Y
23 C 9/11 A, 5-11 EO multibranched 1 1 000 0,001 0,001 0,05 R O
24 C 10 A, 5-11 EO multibr.(Trimer-propen-oxo-alcohol) 1 1 000 0,001 0,001 0,05 R Y
25 C 12/15 A, 2-6 EO predominantly linear 0,43 1 000 0,00043 0,18 50 0,0036 0,05 R Y
26 C 12/14 5-8 EO 1 t-BuO (endcapped) 0,23 1 000 0,00023 0,18 100 0,0018 0,05 R O
27 C 12/15 A, 3-12 EO multibranched 1 1 000 0,001 3,2 100 0,032 0,05 R O
28 C 12/15 (mean value C < 14) A, >6-9 EO 0,63 1 000 0,00063 0,24 10 0,024 0,05 R Y
29 C 12/15 (mean value C > 14) A, >6-9 EO 0,4 1 000 0,0004 0,17 10 0,017 0,05 R Y
30 C 12/15 A, > 9-12 EO 1,1 1 000 0,0011 0,017 0,05 R Y
31 C 12/15 A >12-20 EO 0,7 1 000 0,0007 0,0007 0,05 R O
32 C 12/15 A > 20-30 EO 13 1 000 0,013 10 100 0,1 0,05 R O
33 C 12/15 A, > 30 EO 130 1 000 0,13 0,13 0,5 I O
34 C 12/18 A, 0-3 EO 0,3 1 000 0,0003 0,0003 0,05 R Y
35 C 12/18 A, 5-10 EO 1 1 000 0,001 0,35 100 0,0035 0,05 R O
36 C 12/18 A, > 10-20 EO 1 1 000 0,001 0,0035 0,05 R O
37 C 16/18 A, 2-8 EO 3,2 1 000 0,0032 0,4 100 0,004 0,05 R Y
38 C 16/18 A, > 9-18 EO 0,72 1 000 0,00072 0,32 10 0,032 0,05 R Y
39 C 16/18 A, 20-30 EO 4,1 1 000 0,0041 0,0041 0,05 R Y
40 C 16/18 A, > 30 EO 30 1 000 0,03 0,03 0,5 I Y
41 C 12-15 A 2-6 EO 2-6 PO 0,78 1 000 0,00078 0,36 100 0,0036 0,05 R O
42 C 10-16 A 0-3 PO 6-7 EO 3,2 5 000 0,00064 1 100 0,01 0,05 R O
43 Glycerin (1-5 EO) cocoate 16 1 000 0,016 6,3 100 0,063 0,05 R Y
44 Glycerin (6-17 EO) cocoate 100 1 000 0,1 0,1 0,05 R Y
45 C 12/14 Glucose amide 13 1 000 0,013 4,3 50 0,086 0,05 R Y
46 C 16/18 Glucose amide 1 1 000 0,001 0,33 50 0,0066 0,05 R Y
47 C 8/10 Alkyl polyglycoside 28 1 000 0,028 5,7 100 0,057 0,05 R Y
48 C 8/12 Alkyl polyglycoside, branched 480 1 000 0,48 100 100 1 0,05 R N
49 C 8/16 or C 12-14 Alkyl polyglycoside 5,3 1 000 0,0053 1 10 0,1 0,05 R Y
50 Coconut fatty acid monoethanolamide 9,5 1 000 0,0095 1 100 0,01 0,05 R Y
51 Coconut fatty acid monoethanolamide 4-5 EO 17 10 000 0,0017 0,0017 0,05 R Y
52 Coconut fatty acid diethanolamide 2 1 000 0,002 0,3 100 0,003 0,05 R O
53 PEG-4 Rapeseed amide 7 5 000 0,0014 0,0014 0,05 R Y
Amphoteric surfactants
60 C 12/15 Alkyl dimethylbetaine 1,7 1 000 0,0017 0,1 100 0,001 0,05 R O
61 Alkyl C 12/18 amidopropylbetaine 1,8 1 000 0,0018 0,09 100 0,0009 0,05 R Y
62 C 12/18 Alkyl amine oxide 0,3 1 000 0,0003 0,0003 0,05 R Y
Cationic surfactants
70 Alkyl trimethyl ammonium salts 0,1 1 000 0,0001 0,046 100 0,00046 0,5 I O
71 Alkyl ester ammonium salts 2,9 1 000 0,0029 1 10 0,1 0,05 R Y
Preservatives
80 1,2-Benzisothiazol-3-one 0,15 1 000 0,00015 0,00015 0,5 I N
81 Benzyl alcohol 360 1 000 0,36 0,36 0,05 R Y
82 5-bromo-5-nitro-1,3-dioxane 0,4 5 000 0,00008 0,00008 1 P O
83 2-bromo-2-nitropropane-1,3-diol 0,78 1 000 0,00078 0,2 100 0,002 0,5 I O
84 Chloroacetamide 55,6 10 000 0,00556 0,00556 1 O O
85 Diazolinidylurea 35 5 000 0,007 0,007 1 P O
86 Formaldehyde 2 1 000 0,002 0,002 0,05 R O
87 Glutaraldehyde 0,31 1 000 0,00031 0,00031 0,05 R O
88 Guanidine, hexamethylene-, homopolymer 0,18 1 000 0,00018 0,024 100 0,00024 1 P O
89 CMI + MIT in mixture 3:1(2) 0,0067 1 000 0,0000067 0,0057 50 0,000114 0,5 I O
90 2-Methyl-2H-isothiazol-3-one (MIT) 0,06 1 000 0,00006 0,00006 0,5 I O
91 Methyldibromoglutaronitrile 0,15 1 000 0,00015 0,00015 0,05 R O
92 e-phtaloimidoperoxyhexanoic acid 0,59 5 000 0,000118 0,000118 1 P O
93 Methyl-, Ethyl- and Propylparaben 15,4 5 000 0,00308 0,00308 0,05 R N
94 o-Phenylphenol 0,92 1 000 0,00092 0,00092 0,05 R O
95 Sodium benzoate 128 1 000 0,128 0,128 0,05 R Y
96 Sodium hydroxy methyl glycinate 36,5 5 000 0,0073 0,0073 1 O O
97 Sodium nitrite 87 10 000 0,0087 0,0087 1 NA NA
98 Triclosan 0,0014 1 000 0,0000014 0,0000014 0,5 I O
Other ingredients
110 Silicon 250 1 000 0,25 0,25 1 P N
111 Paraffin 1 000 10 000 0,1 0,1 1 P O
112 Glycerol 4 400 5 000 0,88 0,88 0,05 R Y
113 Phosphate, as STPP 1 000 1 000 1 1 0,15 NA NA
114 Zeolite (Insoluble Inorganic) 1 000 1 000 1 175 50 3,5 1 NA NA
115 Citrate and citric acid 825 1 000 0,825 80 50 1,6 0,05 R Y
116 Polycarboxylates 200 1 000 0,2 106 10 10,6 1 P N
117 Nitrilotriacetat (NTA) 494 1 000 0,494 64 50 1,28 0,5 I O
118 EDTA 121 1 000 0,121 22 50 0,44 0,5 I N
119 Phosphonates 650 1 000 0,65 25 50 0,5 1 P N
120 EDDS 320 1 000 0,32 32 50 0,64 0,05 R N
121 Clay (Insoluble Inorganic) 1 000 1 000 1 1 1 NA NA
122 Carbonates 250 1 000 0,25 0,25 0,15 NA NA
123 Fatty acids C ≥ 14 3,7 5 000 0,00074 0,00074 0,05 R Y
124 Silicates 250 1 000 0,25 0,25 1 NA NA
125 Polyasparaginic acid, Na-salt 410 1 000 0,41 0,41 0,05 R N
126 Perborates (as Boron) 14 1 000 0,014 0,014 1 NA NA
127 Percarbonate (See carbonate) 250 1 000 0,25 0,25 0,15 NA NA
128 Tetraacetylethylenediamine (TAED) 250 1 000 0,25 500 100 5 0,05 R O
129 C 1-C 4 alcohols 1 000 1 000 1 1 0,05 R Y
130 Mono-, di- and triethanol amine 90 1 000 0,09 0,78 100 0,0078 0,05 R Y
131 Polyvinylpyrrolidon (PVP) 1 000 1 000 1 1 0,5 I N
132 Carboxymethylcellulose (CMC) 250 5 000 0,05 0,05 0,5 I N
133 Sodium and magnesium sulphate 1 000 1 000 1 100 100 1 1 NA NA
134 Calcium- and sodiumchloride 1 000 1 000 1 100 100 1 1 NA NA
135 Urea 1 000 5 000 0,2 0,2 1 NA NA
136 Silicon dioxide, quartz (Insoluble inorganic) 1 000 1 000 1 1 1 NA NA
137 Polyethylene glycol, MW>4000 1 000 10 000 0,1 0,1 1 P N
138 Polyethylene glycol, MW<4000 1 000 10 000 0,1 0,1 1 P O
139 Cumene-, Xylene- and Toluene sulphonates 66 10 000 0,0066 0,0066 0,5 I N
140 Na-/Mg-/KOH 30 1 000 0,03 0,03 0,05 NA NA
141 Enzymes/proteins 25 5 000 0,005 0,005 0,05 R Y
142 Perfume, if not other specified(*2) 2 1 000 0,002 0,002 0,5 I N
143 Dyes, if not other specified(*2) 10 1 000 0,01 0,01 1 P N
144 Starch 100 1 000 0,1 0,1 0,05 R Y
145 Anionic polyester 655 1 000 0,655 0,655 1 P N
146 PVNO/PVPI 530 1 000 0,53 0,53 1 P N
147 Zn Ftalocyanin sulphonate 0,2 1 000 0,0002 0,16 100 0,0016 1 P N
148 Iminodisuccinat 81 1 000 0,081 17 100 0,17 0,05 R N
149 FWA 1 11 1 000 0,011 10 100 0,1 1 P N
150 FWA 5 10 1 000 0,01 1 10 0,1 1 P N
151 1-decanol 2,3 5 000 0,00046 0,00046 0,05 R O
152 Methyl laurate 1 360 10 000 0,136 0,136 0,05 R O
153 Formic acid (Ca salt) 100 1 000 0,1 0,1 0,05 R Y
154 Adipic acid 31 1 000 0,031 0,031 0,05 R O
155 Maleic acid 106 1 000 0,106 0,106 0,05 R Y
156 Malic acid 106 1 000 0,106 0,106 0,05 R O
157 Tartaric acid 200 10 000 0,02 0,02 0,05 R O
158 Phosphoric acid 138 1 000 0,138 0,138 0,15 NA NA
159 Oxalic acid 128 5 000 0,0256 0,0256 0,05 R O
160 Acetic acid 30 1 000 0,03 0,03 0,05 R Y
161 Lactic acid 130 1 000 0,13 0,13 0,05 R Y
162 Sulphamic acid 75 1 000 0,075 0,075 1 NA NA
163 Salicylic acid 46 1 000 0,046 0,046 0,15 R O
164 Glycollic acid 141 5 000 0,0282 0,0282 0,05 R O
165 Glutaric acid 208 5 000 0,0416 0,0416 0,05 R O
166 Malonic acid 95 5 000 0,019 0,019 0,05 R O
167 Ethylene glycol 6 500 1 000 6,5 6,5 0,05 R Y
168 Ethylene glycol monobutyl ether 747 5 000 0,1494 0,1494 0,05 R O
169 Diethylene glycol 4 400 10 000 0,44 0,44 0,15 I Y
170 Diethylene glycol monomethyl ether 500 1 000 0,5 0,5 0,5 I O
171 Diethylene glycol monoethyl ether 3 940 5 000 0,788 0,788 0,05 R O
172 Diethylene glycol monobutyl ether 1 254 1 000 1,254 1,254 0,05 R O
173 Diethylene glycol dimethylether 2 000 10 000 0,2 0,2 0,5 I O
174 Propylene glycol 32 000 1 000 32 32 0,15 R Y
175 Propylene glycol monomethyl ether 12 700 5 000 2,54 2,54 0,05 R O
176 Propylene glycol monobutylether 748 5 000 0,1496 0,1496 0,05 R O
177 Dipropylene glycol 1 625 10 000 0,1625 0,1625 0,05 R O
178 Dipropylene glycol monomethyl ether 1 919 5 000 0,3838 0,3838 0,05 R O
179 Dipropylene glycol monobutylether 841 5 000 0,1682 0,1682 0,05 R O
180 Dipropylene glycol dimethylether 1 000 5 000 0,2 0,2 0,5 I O
181 Triethylene glycol 4 400 1 000 4,4 4,4 0,5 I O
182 Tall oil 1,8 1 000 0,0018 0,0018 0,5 I O
183 Ethylenebisstearamides 140 5 000 0,028 0,028 0,5 I O
184 Sodium gluconate 10 000 10 000 1 1 0,05 R O
185 Glycol distearate 100 5 000 0,02 0,02 0,5 I O
186 Hydroxyl ethyl cellulose 209 5 000 0,0418 0,0418 1 P O
187 Hydroxy propyl methyl cellulose 188 5 000 0,0376 0,0376 1 P O
188 1-methyl-2-pyrrolidone 500 1 000 0,5 0,5 0,05 R O
189 Xanthan gum 490 1 000 0,49 0,49 0,05 R O
190 Trimethyl Pentanediol mono-isobutyrate 18 1 000 0,018 3,3 100 0,033 0,05 R O
191 Benzotriazole 29 1 000 0,029 0,029 1 P O
192 Piperidinol-propanetricarboxylate salt 100 1 000 0,1 120 100 1,2 0,5 I O
193 Diethylaminopropyl-DAS 120 1 000 0,12 120 100 1,2 1 P O
194 Methylbenzamide-DAS 120 1 000 0,12 120 100 1,2 0,5 I O
195 Pentaerythritol-tetrakis-phenol-propionate 38 1 000 0,038 0,038 1 P O
196 Block polymers 100 5 000 0,02 0,02 1 P N
197 Denatonium benzoate 13 5 000 0,0026 0,0026 1 O O
198 Succinate 374 10 000 0,0374 0,0374 0,05 R O
199 Polyaspartic acid 528 1 000 0,528 0,528 0,05 R N
Insoluble inorganic ingredient with very low, or no ability to dissolve in water.
List of abbreviations:SF(acute)=safety factor for acute toxicity.TF(acute)=toxicity factor based on acute toxicity on aquatic organisms.SF(chronic)=xafety factor for chronic toxicity.TF(chronic)=toxicity factor based on chronic toxicity on aquatic organisms.DF=degradation factor.Aerobic degradation:R=readily biodegradable according to OECD guidelines.I=Iinherently biodegradable according to OECD guidelines.P=persistent. The ingredient has failed the test for inherent biodegradability.O=the ingredient has not been tested.NA=not applicable.Anaerobic degradation:Y=biodegradable under anaerobic conditions.N=not biodegradable under anaerobic conditions.O=the ingredient has not been tested.NA=not applicable. SF(acute) = safety factor for acute toxicity. TF(acute) = toxicity factor based on acute toxicity on aquatic organisms. SF(chronic) = xafety factor for chronic toxicity. TF(chronic) = toxicity factor based on chronic toxicity on aquatic organisms. DF = degradation factor. R = readily biodegradable according to OECD guidelines. I = Iinherently biodegradable according to OECD guidelines. P = persistent. The ingredient has failed the test for inherent biodegradability. O = the ingredient has not been tested. NA = not applicable. Y = biodegradable under anaerobic conditions. N = not biodegradable under anaerobic conditions. O = the ingredient has not been tested. NA = not applicable.
SF(acute) = safety factor for acute toxicity.
TF(acute) = toxicity factor based on acute toxicity on aquatic organisms.
SF(chronic) = xafety factor for chronic toxicity.
TF(chronic) = toxicity factor based on chronic toxicity on aquatic organisms.
DF = degradation factor.
R = readily biodegradable according to OECD guidelines.
I = Iinherently biodegradable according to OECD guidelines.
P = persistent. The ingredient has failed the test for inherent biodegradability.
O = the ingredient has not been tested.
NA = not applicable.
Y = biodegradable under anaerobic conditions.
N = not biodegradable under anaerobic conditions.
O = the ingredient has not been tested.
NA = not applicable.
SF(acute) = safety factor for acute toxicity.
TF(acute) = toxicity factor based on acute toxicity on aquatic organisms.
SF(chronic) = xafety factor for chronic toxicity.
TF(chronic) = toxicity factor based on chronic toxicity on aquatic organisms.
DF = degradation factor.
R = readily biodegradable according to OECD guidelines.
I = Iinherently biodegradable according to OECD guidelines.
P = persistent. The ingredient has failed the test for inherent biodegradability.
O = the ingredient has not been tested.
NA = not applicable.
Y = biodegradable under anaerobic conditions.
N = not biodegradable under anaerobic conditions.
O = the ingredient has not been tested.
NA = not applicable.
CDV= 1000 * Σdosage(i)*DF(i)/TF(i)
Dosage(i) = dosage of ingredient i, expressed in g/wash, or in some cases as g/100 g product.
DF(i) = degradation factor for ingredient i.
TF(i) = toxicity factor for ingredient i.
— Calculate the median value within each trophic level (fish, crustaceans or algae) using validated test results for chronic toxicity. If several test results are available for one species within a trophic level, a median for the species shall be calculated first, and these median values shall be used when calculating the median value for the trophic level.
— The chronic toxicity factor (TFchronic) is the lowest median of the trophic levels calculated.
— The TFchronicshall be used when calculating the critical dilution volume criterion.
— Calculate the median value within each trophic level (fish, crustaceans or algae) using validated test results for acute toxicity. If several test results are available for one species within a trophic level, a median for the species shall be calculated first, and these median values shall be used when calculating the median value for the trophic level.
— The acute toxicity factor (TFacute) is the lowest median of the trophic levels.
— The TFacuteshall be used when calculating the critical dilution volume criterion.
Data Safety factor (SF) Toxicity factor (TF)
One short-term L(E)C50 10 000 Toxicity/10 000
Two short-term L(E)C50 from species representing two trophic levels (fish and/or crustaceans and/or algae) 5 000 Toxicity/5 000
At least one short-term L(E)C50 from each of three trophic levels of the base-set 1 1 000 Toxicity/1 000
One long-term NOEC (fish or crustaceans) 100 Toxicity/100
Two long-term NOEC from species representing two trophic levels (fish and/or crustaceans and/or algae) 50 Toxicity/50
Long-term NOEC from at least three species (normally fish, crustaceans and algae) representing three trophic levels 10 Toxicity/10
— The base set for testing the toxicity of substances towards aquatic organisms consists of acute tests with fish, daphnia and algae.
DF
Readily biodegradable(*3) 0,05
Readily biodegradable(*4) 0,15
Inherently biodegradable 0,5
Persistent 1
Category Label
Anaerobically not biodegradable, i.e. tested and found not biodegradable. N
Anaerobically biodegradable, i.e. tested and found biodegradable or not tested but demonstrated through analogy considerations etc. Y
Not tested for anaerobic biodegradability. 0
Category Label
Readily biodegradable R
Inherently biodegradable, but not readily biodegradable I
Persistent P
Not tested for aerobic biodegradability O
(#) Due to a lack of toxicity results the TF has been calculated as an average of the values of C 12/14 Alkyl sulphate (AS) and C 16/18 Alkyl sulphate (AS).
(§) 5-Chloro-2-Methyl-4-isothiazolin-3-one and 2-Methyl-4-isothiazolin-3-one in mixture 3: 1
— The same volume of water must be used in all subtests. The volume must be determined in litres to one decimal point.
— The water hardness, specified inOdH, and the calcium-magnesium-ratio must be known.
— The water temperature must be the same for all subtests. It shall be measured at the start and kept constant throughout the test. However, a decrease of the water temperature during the test is acceptable, if the same temperature decrease is documented for all subtests.
— The reference product may either be a market-leading product or a generic formulation.
— If a market-leading reference product is used, it shall be one of the three to four products with the highest sales volume on the market in a region, where the eco-labelled product is to be marketed. Furthermore, the market-leading reference product must be approved by the competent body, and the trade name must be available to the public.
— If a generic reference product is used, it must have a composition, which is representative of the products on the market. Furthermore, the generic reference product must be approved by the competent body and the exact formulation must be commonly available free of charge.
— The dosage of test product and reference product shall be the recommended dosage in all tests, normalised to the given volume of water and weighed in grams to one decimal point. If no recommended dosage is stated for the reference product, the same dosage must be used for both the test product and the reference product.
— If a dosage interval is given, the lowest recommended dosage must be used for the test.
— The detergent must be mixed and completely dissolved in the water.
— At least one type of soil, consisting primarily of fresh animal fat and vegetable fat, must be used.
— The same soil must be used for all subtests.
— The origin or chemical composition of the soil, e.g. olive oil, beef tallow, etc., must be described in detail.
— The soil must be homogenous and of even consistency.
— Enough soil for the entire test must be prepared in one batch.
— The quantity of soil applied to a substrate, e.g. plates or dishes, or to the washing-water must be the same in all subtests and must be weighed in grams to one decimal point.
— The test and reference products must be made anonymous to the person(s) performing the test.
— The elements and stages included in each subtest must be decided in advance and must be identical for each subtest.
— The temperature and relative humidity of the room must be measured and kept constant in all subtests.
— A fixed procedure for application of soil, allowing sufficient time for drying, must be determined in advance.
— A fixed procedure for manual dishwashing or removal of soil by machinery must be described in advance
— At least five subtests must be performed with both the test and reference product, and at least one test must be performed with water without addition of detergent.
— The test must be capable of generating results that provide a measure of capacity. The capacity must be expressed in grams of soil removed per five litres of water before reaching a predefined point of saturation. The point of saturation can for example be when a cleaning effect is no longer observed, when soil is floating at the surface of the water, when the foam layer is not completely covering the surface, or when there is no visible foam.
— The test must be capable of generating results that provide a measure of the cleanness. Cleanness can be measured visually, optically or by means of another relevant method. The method of measurement, including a possible scoring system, must be decided in advance.
— A positive result of a test round is obtained when the capacity and cleanness are as good as or better for the test product compared with the reference product.
— The test product is considered to have fulfilled the performance requirements when positive results are obtained in at least 80 % of the test rounds. As an alternative, the applicant may use statistical methods and demonstrate with a one-sided 95 % confidence range that the test product is as good as or better than the reference product in at least 80 % of the test rounds.
— It shall also be shown that the test product has a better cleaning ability than that of pure water.
— description of how the test and reference products were made anonymous to the person(s) performing the test,
— specification of the temperature and humidity in the test room and details describing how the test person(s) ensured that these conditions were kept constant in all subtests,
— description of the composition of the soil and of the procedure used to ensure that the soil was of a homogenous and even consistency,
— specification of the hardness of the water, and how it was achieved, and specification of the calcium-magnesium ratio,
— specification of the quantity of water used in the subtests and specification of how the water temperature requirement was fulfilled,
— specification of the results of the weighing of the hand dishwashing detergent in each subtest and description of the procedure for dissolving the product in the water,
— description of the procedure for adding the soil to either a substrate (e.g. plates or dishes) or to the washing water,
— specification of the results of the weighing of soil in each subtest,
— description of the other elements and stages in each individual subtest,
— description of how capacity and cleanness were measured,
— raw data from all test rounds stated in terms of capacity and cleanness,
— final results including the results of the water test (in which no detergent is used) and, if applicable, a statistical evaluation of the data.
THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Regulation (EC) No 1980/2000 of the European Parliament and of the Council of 17 July 2000 on a revised Community eco-label award scheme ((1)), and in particular the second subparagraph of Article 6(1) thereof,
After consulting the European Union Eco-Labelling Board,
(1) Under Regulation (EC) No 1980/2000 the Community eco-label may be awarded to a product possessing characteristics which enable it to contribute significantly to improvements in relation to key environmental aspects.
(2) Regulation (EC) No 1980/2000 provides that specific eco-label criteria, drawn up on the basis of the criteria drafted by the European Union Eco-Labelling Board, are to be established according to product groups.
(3) It also provides that the review of the eco-label criteria, as well as of the assessment and verification requirements related to the criteria, is to take place in good time before the end of the period of validity of the criteria specified for the product group concerned.
(4) It is appropriate, in order to take account of scientific and market developments, to revise the ecological criteria established by Commission Decision 2001/607/EC of 19 July 2001 establishing the ecological criteria for the award of the Community eco-label to hand dishwashing detergents ((2)).
(5) Furthermore, in order to specify that products for both private and professional use are covered, it is necessary to modify the definition of the product group laid down in that Decision.
(6) In the interests of clarity, Decision 2001/607/EC should therefore be replaced.
(7) The revised ecological criteria should be valid for a period of four years.
(8) It is appropriate to allow a transitional period of not more than 12 months for applicants whose products have been awarded the eco-label before the date of notification of this Decision or who have applied for such an award before that date, so that they have sufficient time to adapt their products to comply with the revised criteria and requirements.
(9) The measures provided for in this Decision are in accordance with the opinion of the Committee instituted by Article 17 of Regulation (EC) No 1980/2000,
HAS ADOPTED THIS DECISION:

Article 1
The product group ‘hand dishwashing detergents’ shall comprise:
‘all detergents intended to be used, to wash by hand, dishes, crockery, cutlery, pots, pans, kitchen utensils and so on’
The product group shall cover products for both private and professional use.

Article 2
In order to be awarded the Community eco-label, for hand dishwashing detergents, under Regulation (EC) No 1980/2000, a detergent must fall within the product group ‘hand dishwashing detergents’ and must comply with the ecological criteria set out in the Annex to this Decision.

Article 3
The ecological criteria for the product group ‘hand dishwashing detergents’, as well as the related assessment and verification requirements, shall be valid until 31 December 2008.

Article 4
For administrative purposes the code number assigned to the product group ‘hand dishwashing detergents’ shall be 019.

Article 5
Decision 2001/607/EC is repealed.

Article 6
Eco-labels awarded before the notification date of this Decision in respect of products falling within the product group ‘hand dishwashing detergents’ may continue to be used until 31 March 2006.
Where applications have been submitted before the notification date of this Decision for award of the eco-label in respect of products falling within the product group ‘hand dishwashing detergents’ those products may be awarded the eco-label under the conditions laid down in Decision 2001/607/EC. In such cases, the eco-label may be used until 31 March 2006.

Article 7
This Decision is addressed to the Member States.

THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Regulation (EC) No 1980/2000 of the European Parliament and of the Council of 17 July 2000 on a revised Community eco-label award scheme ((1)), and in particular the second subparagraph of Article 6(1) thereof,
After consulting the European Union Eco-Labelling Board,
(1) Under Regulation (EC) No 1980/2000 the Community eco-label may be awarded to a product possessing characteristics which enable it to contribute significantly to improvements in relation to key environmental aspects.
(2) Regulation (EC) No 1980/2000 provides that specific eco-label criteria, drawn up on the basis of the criteria drafted by the European Union Eco-Labelling Board, are to be established according to product groups.
(3) It also provides that the review of the eco-label criteria, as well as of the assessment and verification requirements related to the criteria, is to take place in good time before the end of the period of validity of the criteria specified for the product group concerned.
(4) It is appropriate, in order to take account of scientific and market developments, to revise the ecological criteria established by Commission Decision 2001/607/EC of 19 July 2001 establishing the ecological criteria for the award of the Community eco-label to hand dishwashing detergents ((2)).
(5) Furthermore, in order to specify that products for both private and professional use are covered, it is necessary to modify the definition of the product group laid down in that Decision.
(6) In the interests of clarity, Decision 2001/607/EC should therefore be replaced.
(7) The revised ecological criteria should be valid for a period of four years.
(8) It is appropriate to allow a transitional period of not more than 12 months for applicants whose products have been awarded the eco-label before the date of notification of this Decision or who have applied for such an award before that date, so that they have sufficient time to adapt their products to comply with the revised criteria and requirements.
(9) The measures provided for in this Decision are in accordance with the opinion of the Committee instituted by Article 17 of Regulation (EC) No 1980/2000,
HAS ADOPTED THIS DECISION:
The product group ‘hand dishwashing detergents’ shall comprise:
‘all detergents intended to be used, to wash by hand, dishes, crockery, cutlery, pots, pans, kitchen utensils and so on’
The product group shall cover products for both private and professional use.
In order to be awarded the Community eco-label, for hand dishwashing detergents, under Regulation (EC) No 1980/2000, a detergent must fall within the product group ‘hand dishwashing detergents’ and must comply with the ecological criteria set out in the Annex to this Decision.
The ecological criteria for the product group ‘hand dishwashing detergents’, as well as the related assessment and verification requirements, shall be valid until 31 December 2008.
For administrative purposes the code number assigned to the product group ‘hand dishwashing detergents’ shall be 019.
Decision 2001/607/EC is repealed.
Eco-labels awarded before the notification date of this Decision in respect of products falling within the product group ‘hand dishwashing detergents’ may continue to be used until 31 March 2006.
Where applications have been submitted before the notification date of this Decision for award of the eco-label in respect of products falling within the product group ‘hand dishwashing detergents’ those products may be awarded the eco-label under the conditions laid down in Decision 2001/607/EC. In such cases, the eco-label may be used until 31 March 2006.
This Decision is addressed to the Member States.

FRAMEWORK

ANNEXIn order to qualify for the eco-label, a hand dishwashing detergent (hereinafter referred to as the product) must fall within the product group as defined in Article 1, and must comply with the criteria of this Annex.
The aims of the criteriaThese criteria aim in particular at promoting:

— | the reduction of discharges of toxic or otherwise polluting substances into the aquatic environment,
— | the reduction or prevention of risks to health or the environment related to the use of hazardous substances,
— | the minimisation of packaging waste,
— | information that will enable the consumer to use the product in the way that is efficient and minimises environmental impact.The criteria are set at levels that promote the labelling of hand dishwashing detergents that have a low environmental impact.
Assessment and verification requirementsThe specific assessment and verification requirements are indicated within each criterion.
Where appropriate, test methods other than those indicated for each criterion may be used if the competent body assessing the application accepts their equivalence.
Where no tests are mentioned, or are mentioned as being for use in verification or monitoring, competent bodies should rely as appropriate on declarations and documentation provided by the applicant and/or independent verifications.
Where appropriate, competent bodies may require supporting documentation and may carry out independent verifications.
Where the applicant is required to provide declarations, documentation, analyses test reports, or other evidence to show compliance with the criteria, it is understood that these may originate from the applicant and/or his supplier(s) and/or their supplier(s), et cetera, as appropriate.
Where ingredients are referred to, this includes substances and preparations.
Appendix I presents the new revised detergent ingredient database (DID list), version 30 June 2004, which contains the most widely used ingredients in detergent formulations. Part A of the DID list shall be used for deriving the data for the calculations of CDVtoxand for the assessment of the biodegradability of surfactants.
Where appropriate, the applicant may use subsequent revisions of the detergent ingredient database as they become available.
For ingredients which are not included in part A of the DID list, the applicant shall, under his own responsibility, apply the procedure as described in the part-B of Appendix I.
For ingredients, which are not listed in the DID list, the applicant may use an approach to provide the necessary documentation of anaerobic degradability described in Appendix II.
The competent bodies are recommended to take into account the implementation of recognised environmental management schemes, such as EMAS or ISO 14001, when assessing applications and monitoring compliance with the criteria in this Annex (Note: It is not required to implement such management scheme).
ECOLOGICAL CRITERIA1. Toxicity to aquatic organismsThe critical dilution volume toxicity (CDVtox) is calculated for each ingredient (i) using the following equation:

CDV tox (ingredient i)
=
weight (i) x DF (i) /
TF chronic (i) x 1000
where weight (i) is the weight of the ingredient (in grams) per recommended dose for 1 litre of dishwashing water, DF (i) is the degradation factor and TF chronic (i) is the toxicity factor of the ingredient (in milligram/litre).
The values of DF and TF chronic shall be as given in the Detergent Ingredient Database list-part A (DID list-part A) (Appendix I). If the ingredient in question is not included in the DID list part A, the applicant shall estimate the values following the approach described in the DID list part B (Appendix I). The CDVtoxis summed for each ingredient, making the CDVtoxfor the product.
The CDVtoxof the recommended dose expressed for 1 litre of dishwashing water shall not exceed 4 200 l.
Assessment and verification:the exact formulation of the product shall be provided to the competent body, together with the details of the CDVtoxcalculations showing compliance with this criterion.
2. Biodegradability of surfactants(a) Ready biodegradability (aerobic)Each surfactant used in the product shall be readily biodegradable.
Assessment and verification: the exact formulation of the product as well as a description of the function of each ingredient shall be provided to the Competent Body. The DID list part A (Appendix I) indicates whether a specific surfactant is aerobically biodegradable or not (the surfactants with an entry of ‘R’ in the column on aerobic biodegradability are readily biodegradable). For surfactants which are not included in the DID list part A, the relevant information from literature or other sources, or appropriate test results, showing that they are aerobically biodegradable shall be provided. The tests for ready biodegradability shall be as referred to in Regulation (EC) No 648/2004 of the European Parliament and of the Council of 31 March 2004 on detergents(1). Surfactants shall be considered as readily biodegradable if the level of biodegradability (mineralisation) measured according to one of the five following tests is at least 60 % within 28 days: CO2headspace test (OECD 310), carbon dioxide (CO2) Evolution Modified Sturm test (OECD 301B; Directive 67/548/EEC Annex V.C.4-C), Closed Bottle test (OECD 301D; Directive 67/548/EEC Annex VC(4E)), Manometric Respirometry (OECD 301F; Directive 67/548/EEC Annex VC(4D)), or MITI (I) test (OECD 301C; Directive 67/548/EEC Annex VC(4F)), or their equivalent ISO tests. Depending on the physical characteristics of the surfactant, one of the following tests might be used to confirm ready biodegradability, if the level of biodegradability is at least 70 % within 28 days: Dissolved Organic Carbon DOC Die-Away (OECD 301A; Directive 67/548/EEC Annex VC(4A)) or Modified OECD Screening DOC Die-Away (OECD 301E; Directive 67/548/EEC Annex VC(4B)), or their equivalent ISO tests. The applicability of test methods based on measurement of dissolved organic carbon needs to be appropriately justified as these methods could give results on the removal and not on the biodegradability. Pre-adaptation is not to be used in tests for aerobic ready biodegradability. The 10 days window principle shall not apply.
(b) Anaerobic biodegradabilityEach surfactant used in the product shall be biodegradable under anaerobic conditions.
Assessment and verification:the exact formulation of the product as well as a description of the function of each ingredient shall be provided to the competent body. The DID list part A (Appendix I) indicates whether a specific surfactant is anaerobically biodegradable or not (the surfactants with an entry of ‘Y’ in the column on anaerobic biodegradability are biodegradable under anaerobic conditions). For surfactants which are not included in the DID list part A, the relevant information from literature or other sources, or appropriate test results, showing that they are anaerobically biodegradable shall be provided. The reference test for anaerobic degradability shall be OECD 311, ISO 11734, ECETOC No 28 (June 1988) or an equivalent test method, with the requirement of a minimum of 60 % ultimate degradability under anaerobic conditions. Test methods simulating the conditions in a relevant anaerobic environment may also be used to document that 60 % ultimate degradability has been attained under anaerobic conditions (see Appendix II).
3. Dangerous, hazardous or toxic substances or preparations
(a) | The following ingredients shall not be included in the product, either as part of the formulation or as part of any preparation included in the formulation:—alkyl phenol ethoxylates (APEOs) and derivatives thereof—EDTA (ethylene-diamine-tetra-acetic acid) and its salts—NTA (nitrilo-tri-acetate)—nitromusks and polycyclic musks, including for example:—musk xylene: 5-tert-butyl-2,4,6-trinitro-m-xylene—musk ambrette: 4-tert-butyl-3-methoxy-2,6-dinitrotoluene—moskene: 1,1,3,3,5-pentamethyl-4,6-dinitroindan—musk tibetine: 1-tert-butyl-3,4,5-trimethyl-2,6-dinitrobenzene—musk ketone: 4′-tert-butyl-2′,6′-dimethyl-3′,5′-dinitroacetaphenone—HHCB (1,3,4,6,7,8-Hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran)—AHTN (6-Acetyl-1,1,2,4,4,7-hexamethyltetralin).Assessment and verification: the applicant shall provide a declaration supported by declarations from manufacturers, as appropriate, confirming that the listed substances have not been included in the product. | — | alkyl phenol ethoxylates (APEOs) and derivatives thereof | — | EDTA (ethylene-diamine-tetra-acetic acid) and its salts | — | NTA (nitrilo-tri-acetate) | — | nitromusks and polycyclic musks, including for example:—musk xylene: 5-tert-butyl-2,4,6-trinitro-m-xylene—musk ambrette: 4-tert-butyl-3-methoxy-2,6-dinitrotoluene—moskene: 1,1,3,3,5-pentamethyl-4,6-dinitroindan—musk tibetine: 1-tert-butyl-3,4,5-trimethyl-2,6-dinitrobenzene—musk ketone: 4′-tert-butyl-2′,6′-dimethyl-3′,5′-dinitroacetaphenone—HHCB (1,3,4,6,7,8-Hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran)—AHTN (6-Acetyl-1,1,2,4,4,7-hexamethyltetralin). | — | musk xylene: 5-tert-butyl-2,4,6-trinitro-m-xylene | — | musk ambrette: 4-tert-butyl-3-methoxy-2,6-dinitrotoluene | — | moskene: 1,1,3,3,5-pentamethyl-4,6-dinitroindan | — | musk tibetine: 1-tert-butyl-3,4,5-trimethyl-2,6-dinitrobenzene | — | musk ketone: 4′-tert-butyl-2′,6′-dimethyl-3′,5′-dinitroacetaphenone | — | HHCB (1,3,4,6,7,8-Hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran) | — | AHTN (6-Acetyl-1,1,2,4,4,7-hexamethyltetralin).
— | alkyl phenol ethoxylates (APEOs) and derivatives thereof
— | EDTA (ethylene-diamine-tetra-acetic acid) and its salts
— | NTA (nitrilo-tri-acetate)
— | nitromusks and polycyclic musks, including for example:—musk xylene: 5-tert-butyl-2,4,6-trinitro-m-xylene—musk ambrette: 4-tert-butyl-3-methoxy-2,6-dinitrotoluene—moskene: 1,1,3,3,5-pentamethyl-4,6-dinitroindan—musk tibetine: 1-tert-butyl-3,4,5-trimethyl-2,6-dinitrobenzene—musk ketone: 4′-tert-butyl-2′,6′-dimethyl-3′,5′-dinitroacetaphenone—HHCB (1,3,4,6,7,8-Hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran)—AHTN (6-Acetyl-1,1,2,4,4,7-hexamethyltetralin). | — | musk xylene: 5-tert-butyl-2,4,6-trinitro-m-xylene | — | musk ambrette: 4-tert-butyl-3-methoxy-2,6-dinitrotoluene | — | moskene: 1,1,3,3,5-pentamethyl-4,6-dinitroindan | — | musk tibetine: 1-tert-butyl-3,4,5-trimethyl-2,6-dinitrobenzene | — | musk ketone: 4′-tert-butyl-2′,6′-dimethyl-3′,5′-dinitroacetaphenone | — | HHCB (1,3,4,6,7,8-Hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran) | — | AHTN (6-Acetyl-1,1,2,4,4,7-hexamethyltetralin).
— | musk xylene: 5-tert-butyl-2,4,6-trinitro-m-xylene
— | musk ambrette: 4-tert-butyl-3-methoxy-2,6-dinitrotoluene
— | moskene: 1,1,3,3,5-pentamethyl-4,6-dinitroindan
— | musk tibetine: 1-tert-butyl-3,4,5-trimethyl-2,6-dinitrobenzene
— | musk ketone: 4′-tert-butyl-2′,6′-dimethyl-3′,5′-dinitroacetaphenone
— | HHCB (1,3,4,6,7,8-Hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran)
— | AHTN (6-Acetyl-1,1,2,4,4,7-hexamethyltetralin).
(b) | Quaternary ammonium salts that are not readily biodegradable shall not be used, either as part of the formulation or as part of any preparation included in the formulation.Assessment and verification: the applicant shall provide documentation showing the biodegradability of any quaternary ammonium salt used.
(c) | No ingredient (substance or preparation) shall be included in the product that is classified with any of the following risk phrases, or any combination thereof, in accordance with Council Directive 67/548/EEC of 27 June 1967 on the approximation of laws, regulations and administrative provisions relating to the classification, packaging and labelling of dangerous substances ((2)) and its amendments or Directive 1999/45/EC of the European Parliament and of the Council of 31 May 1999 concerning the approximation of the laws, regulations and administrative provisions of the Member States relating to the classification, packaging and labelling of dangerous preparations ((3)) and its amendments:R40 (limited evidence of a carcinogenic effect),R45 (may cause cancer),R46 (may cause heritable genetic damage),R49 (may cause cancer by inhalation),R68 (possible risks of irreversible effects),R50-53 (very toxic to aquatic organism and may cause long term adverse effects in the aquatic environment),R51-53 (toxic to aquatic organism and may cause long term adverse effects in the aquatic environment),R59 (dangerous to the ozone layer),R60 (may impair fertility),R61 (may cause harm to the unborn child),R62 (possible risk of impaired fertility),R63 (possible risk of harm to the unborn child),R64 (may cause harm to breastfed babies).Specific requirements are prescribed for biocides, either as part of the formulation or as part of any preparation included in the formulation (see criterion on biocides below).The above requirements shall apply to each ingredient (substance or preparation) that exceeds 0,01 % by weight of the final product. This includes also each ingredient of any preparation used in the formulation that exceeds 0,01 % by weight of the final product.Assessment and verification: copies of the material safety data sheets shall be provided for all ingredients (whether substances or preparations). A declaration prepared by the manufacturer of ingredients and showing compliance with this criterion shall be provided by the applicant. | | R40 (limited evidence of a carcinogenic effect), | | R45 (may cause cancer), | | R46 (may cause heritable genetic damage), | | R49 (may cause cancer by inhalation), | | R68 (possible risks of irreversible effects), | | R50-53 (very toxic to aquatic organism and may cause long term adverse effects in the aquatic environment), | | R51-53 (toxic to aquatic organism and may cause long term adverse effects in the aquatic environment), | | R59 (dangerous to the ozone layer), | | R60 (may impair fertility), | | R61 (may cause harm to the unborn child), | | R62 (possible risk of impaired fertility), | | R63 (possible risk of harm to the unborn child), | | R64 (may cause harm to breastfed babies).
| R40 (limited evidence of a carcinogenic effect),
| R45 (may cause cancer),
| R46 (may cause heritable genetic damage),
| R49 (may cause cancer by inhalation),
| R68 (possible risks of irreversible effects),
| R50-53 (very toxic to aquatic organism and may cause long term adverse effects in the aquatic environment),
| R51-53 (toxic to aquatic organism and may cause long term adverse effects in the aquatic environment),
| R59 (dangerous to the ozone layer),
| R60 (may impair fertility),
| R61 (may cause harm to the unborn child),
| R62 (possible risk of impaired fertility),
| R63 (possible risk of harm to the unborn child),
| R64 (may cause harm to breastfed babies).4. Biocides
(a) | The product may only include biocides in order to preserve the product, and in the appropriate dosage for this purpose alone. This does not refer to surfactants, which may also have biocidal properties.Assessment and verification: copies of the material safety data sheets of any preservatives added shall be provided, together with information on their exact concentration in the final product. The manufacturer or supplier of the preservatives shall provide information on the dosage necessary to preserve the product.
(b) | It is prohibited to claim or suggest on the packaging or by any other communication that the hand dishwashing product has an antimicrobial action.Assessment and verification: the texts and layouts used on each type of packaging and/or an example of each different type of packaging shall be provided to the competent body.
(c) | Biocides, either as part of the formulation or as part of any preparation included in the formulation, that are used to preserve the product and that are classified with R50-53 or R51-53 risk phrases, in accordance with Directive 67/548/EEC and its amendments or Directive 1999/45/EC, are permitted but only if they are not potentially bioaccumulative. In this context, a biocide is considered to be potentially bioaccumulative if the log Pow(log octanol/water partition coefficient) ≥ 3,0 (unless the experimentally determined BCF ≤ 100).The concentration of biocides in the final product shall not exceed the maximum authorised concentration in Council Directive 76/768/EEC of 27 July 1976 on the approximation of the laws of the Member States relating to cosmetic products(4)and its subsequent amendments.Assessment and verification:copies of the material safety data sheets shall be provided for all biocides, together with a documentation of the concentrations of the biocides in the final product.5. Dyes or colouring agentsAny dyes or colouring agents used in the product must be permitted by Directive 76/768/EEC and its subsequent amendments, or must be permitted by European Parliament and Council Directive 94/36/EC of 30 June 1994 on colours for use in foodstuffs ((5)) and its subsequent amendments, or must be characterised by environmental properties that do not imply classification with R5053 or R51-53 risk phrases, in accordance with Directive 67/548/EEC and its amendments.
Assessment and verification: a declaration of compliance with this criterion shall be provided to the competent body, together with a full list of all dyes or colouring agents used.
6. Fragrances
(a) | The product shall not contain perfumes containing nitro-musks or polycyclic musks (as specified in the criterion 3a).
(b) | Any ingredients added to the product as a fragrance must have been manufactured and/or handled in accordance with the code of practice of the International Fragrance Association.
(c) | Fragrances shall not be used in hand dishwashing detergents for professional use.Assessment and verification: a declaration of compliance with each part of this criterion shall be provided to the competent body.
7. Sensitising substancesThe product shall not be classified with R42 (may cause sensitisation by inhalation) and/or R43 (may cause sensitisation by skin contact) risk phrases, in accordance with Directive 1999/45/EC and its amendments.
The concentration of any substance or ingredient classified with R42 (may cause sensitisation by inhalation) and/or R43 (may cause sensitisation by skin contact) risk phrases, in accordance with Directive 67/548/EEC and its amendments or Directive 1999/45/EC and its amendments, shall not exceed 0,1 % by weight of the final product.
Assessment and verification: the exact concentrations of all ingredients that are classified as R42 and/or R43 shall be provided to the competent body, together with copies of the material safety data sheets.
8. Harmful or corrosive propertiesThe product shall not be classified as ‘Harmful’ (Xn) or ‘Corrosive’ (C) according to Directive 1999/45/EC.
Assessment and verification: the exact concentrations of all substances used in the product, either as part of the formulation or as part of any preparation included in the formulation, that are classified as ‘Harmful’ (Xn) or ‘Corrosive’ (C) shall be provided to the Competent Body, together with copies of the material safety data sheets.
9. Packaging requirements
(a) | The primary packaging, except for the cap, shall have a volumetric coefficient of packaging (VCP) less than or equal to 1,9. This criterion does not apply if the primary packaging is made up of 50 % or more recycled material.VCP is equal to the volume of the smallest rectangular solid (rectangular parallelepiped) that can contain the packaging divided by the volume of the product contained in the packaging.
(b) | If the primary packaging is made of recycled material, any indication of this on the packaging shall be in conformity with the ISO 14021 standard ‘Environmental labels and declarations — Self declared claims (type II environmental labelling)’.
(c) | The primary packaging parts shall be easily separable into mono-material parts.
(d) | Plastics that are used for the main container shall be marked according to European Parliament and Council Directive 94/62/EC of 20 December 1994 on packaging and packaging waste(6), or DIN 6120 part 1 and 2 in connection with DIN 7728 part 1.Assessment and verification: data on the packaging, and/or a sample thereof if appropriate, shall be provided to the competent body, together with a declaration of compliance with each part of this criterion.
FITNESS FOR USE10. Fitness for useThe product shall be fit for use, meeting the needs of the consumers.
The cleaning ability must be equivalent to or better than that of a market-leading or generic reference product (see Appendix III), approved by a competent body, and better than pure water.
The cleaning capacity must be equivalent to or better than that of a market-leading or generic reference product, approved by a competent body.
Assessment and verification: the cleaning ability and cleaning capacity must be tested by means of an adequate and justifiable laboratory performance test carried out within specified parameters as stated in the framework described in Appendix III.
CONSUMER INFORMATION11. User instructionsThe product shall bear the following information on the packaging:

(a) | ‘To wash your dishes in the most efficient way, to save water and energy, and to protect the environment, do not use running water but immerse the dishes, and use the recommended dosage. You can wash most efficiently without lots of foam’ (or equivalent text);
(b) | The information below shall appear on the packaging in a reasonably sufficient size and against a visible background. The use of pictograms is voluntary.Text of imageRecommended dosage for 5 litres of dishwashing water:not very dirty x ml (y tea spoons) of productdirty z ml (w tea spoons) of productwhere x, y, z and w have to be defined by the applicant and/or the manufacturer.The measure used in the above pictogram shall be millilitres. A second well-known metric, such as teaspoons, shall additionally be given in brackets (as in the pictogram above). However, if the packaging has an efficient and convenient dosing system that can provide an equally reliable dosage, an alternative metric (e.g. capfuls, squirts, or other) may be used;
(c) | an indication of the approximate number of washes that the consumer can perform with one bottle is recommended but voluntary.This is calculated by dividing the volume of the product by the dosage required for 5 l of dishwashing detergent for dirty dishes (as indicated in the pictogram above);
(d) | Regulation (EC) No 648/2004 shall be applied;
(e) | ‘For more information visit the EU eco-label website: http://europa.eu.int/ecolabel’ (or equivalent text).Assessment and verification: a sample of the product packaging, including the label, shall be provided to the competent body, together with a declaration of compliance with each part of this criterion.
12. Information appearing on the eco-labelBox 2 of the eco-label shall contain the following text:

— | reduced impact on aquatic life,
— | reduced use of hazardous substances,
— | clear user instructions.
(1)
OJ L 104, 8.4.2004, p. 1.
(2)
OJ 196, 16.8.1967, p. 1.
(3)
OJ L 200, 30.7.1999, p. 1.
(4)
OJ L 262, 27.9.1976, p. 169.
(5)
OJ L 237, 10.9.1994, p. 13.
(6)
OJ L 365, 31.12.1994, p. 10.

Pending: 32005D0263

2.4.2005 EN Official Journal of the European Union L 85/58
(1) Pursuant to Article 6(9) of Directive 94/55/EC, Member States must give the Commission an advance notification on their derogations for the first time by 31 December 2002 or until two years after the last date of application of the amended versions of the Annexes to the Directive.
(2) Certain Member States had notified the Commission by 31 December 2002 of their wish to adopt derogations from Directive 94/55/EC. By Decision 2003/635/EC of 20 August 2003 authorising Member States pursuant to Directive 94/55/EC to adopt certain derogations with regard to the transport of dangerous goods by road(2), the Commission authorised the adoption by the Member States of the derogations listed in Annexes I and II to that Decision.
(3) Commission Directive 2003/28/EC(3)amended Annexes A and B to Directive 94/55/EC. By virtue of Directive 2003/28/EC Member States had to bring into force national legislation no later than 1 July 2003, the last date of application referred to in Article 6(9) of Directive 94/55/EC being 30 June 2003.
(4) A few Member States notified their wish to adopt derogations. The Commission has examined the notifications for compliance with the conditions laid down in Article 6(9) of Directive 94/55/EC and has approved them. Those Member States should therefore be authorised to adopt the derogations in question.
(5) By the same occasion, it is considered desirable to assemble all the derogations authorised to date in a single decision. Decision 2003/635/EC should therefore be repealed and replaced.
(6) To make sure that the situation of the derogations is updated regularly, the Commission shall propose a comprehensive update of all existing derogations at least every five years.
(7) The measures provided for in this Decision are in accordance with the opinion of the Committee on the transport of dangerous goods, set up by Article 9 of Directive 94/55/EC,
(1) Not more than 25 kg explosive substances under group D are being transported.
(2) Not more than 200 pieces of detonators under group B are being transported.
(3) Detonators and explosive substances must be packed separately in UN-certified packaging in accordance with the rules in Directive 2000/61/EC amending Directive 94/55/EC.
(4) The distance between packaging that contains detonators and packaging that contains explosive substances must be at least 1 meter. This distance has to be observed even after a sudden application of the brakes. Packaging containing explosive substances and packaging containing detonators must be placed in a way that makes it possible quickly to remove them from the vehicle.
(5) All other rules concerning transport of dangerous goods by road must be observed.
1. Explosives allocated on classification to UN Numbers 0029, 0030, 0042, 0065, 0081, 0082, 0104, 0241, 0255, 0267, 0283, 0289, 0290, 0331, 0332, 0360, or 0361 may be carried in the same vehicle with the dangerous goods allocated on classification the UN Number 1942. The quantity of UN 1942 permitted to be carried shall be limited by deeming it to be an explosive of 1.1D;
2. Explosives allocated on classification to UN Number 0191, 0197, 0312, 0336, 0403, 0431, or 0453 may be carried in the same vehicle with dangerous goods (except flammable gases, infectious substances and toxic substances) in transport category 2 or dangerous goods in transport category 3, or any combination of them, provided the total mass or volume of dangerous goods in transport category 2 does not exceed 500 kg or l and the total net mass of such explosives does not exceed 500 kg;
3. Explosives of 1,4G may be carried with flammable liquids and flammable gases in transport category 2 or non-flammable, non-toxic gases in transport category 3, or in any combination of them in the same vehicle, provided the total mass or volume of dangerous goods when added together does not exceed 200 kg or litres and the total net mass of explosives does not exceed 20 kg.
4. Explosive articles allocated on classification to UN Numbers 0106, 0107 or 0257 may be carried with explosive articles in Compatibility Group D, E or F for which they are components. The total quantity of explosives of UN Numbers 0106, 0107 or 0257 shall not exceed 20 kg.
1. Vehicles must either:(a)be placarded according to the applicable provisions of ADR paragraph 5.3.2; or(b)in the case of a vehicles of less than 3 500 kg weight, carrying less than 10 packages containing non-fissile or fissile excepted radioactive material and where the sum of the transport indexes of these packages do not exceed 3, may alternatively carry a notice conforming to the requirements of paragraph 2. (a) be placarded according to the applicable provisions of ADR paragraph 5.3.2; or (b) in the case of a vehicles of less than 3 500 kg weight, carrying less than 10 packages containing non-fissile or fissile excepted radioactive material and where the sum of the transport indexes of these packages do not exceed 3, may alternatively carry a notice conforming to the requirements of paragraph 2.
(a) be placarded according to the applicable provisions of ADR paragraph 5.3.2; or
(b) in the case of a vehicles of less than 3 500 kg weight, carrying less than 10 packages containing non-fissile or fissile excepted radioactive material and where the sum of the transport indexes of these packages do not exceed 3, may alternatively carry a notice conforming to the requirements of paragraph 2.
(a) be placarded according to the applicable provisions of ADR paragraph 5.3.2; or
(b) in the case of a vehicles of less than 3 500 kg weight, carrying less than 10 packages containing non-fissile or fissile excepted radioactive material and where the sum of the transport indexes of these packages do not exceed 3, may alternatively carry a notice conforming to the requirements of paragraph 2.
2. For the purposes of paragraph 1, the notice to be displayed in a vehicle while it is carrying radioactive material shall conform to the following:(a)It shall be not less than 12 cm square. All lettering on the notice shall be black, bold and legible. All lettering shall also be embossed or stamped. The capital letters in the word ‘RADIOACTIVE’ shall be not less than 12 mm high and all other capital letters shall be not less than 5 mm high.(b)It shall be fireproof to the extent that the words on the notice shall remain legible after exposure to a fire involving the vehicle.(c)It shall be securely posted in the vehicle in a position where it is plainly visible to the driver, but does not obstruct his view of the road and shall be exhibited only when the vehicle is carrying radioactive material.(d)It shall be in an agreed form and shall state the name, address and telephone number for use in emergencies. (a) It shall be not less than 12 cm square. All lettering on the notice shall be black, bold and legible. All lettering shall also be embossed or stamped. The capital letters in the word ‘RADIOACTIVE’ shall be not less than 12 mm high and all other capital letters shall be not less than 5 mm high. (b) It shall be fireproof to the extent that the words on the notice shall remain legible after exposure to a fire involving the vehicle. (c) It shall be securely posted in the vehicle in a position where it is plainly visible to the driver, but does not obstruct his view of the road and shall be exhibited only when the vehicle is carrying radioactive material. (d) It shall be in an agreed form and shall state the name, address and telephone number for use in emergencies.
(a) It shall be not less than 12 cm square. All lettering on the notice shall be black, bold and legible. All lettering shall also be embossed or stamped. The capital letters in the word ‘RADIOACTIVE’ shall be not less than 12 mm high and all other capital letters shall be not less than 5 mm high.
(b) It shall be fireproof to the extent that the words on the notice shall remain legible after exposure to a fire involving the vehicle.
(c) It shall be securely posted in the vehicle in a position where it is plainly visible to the driver, but does not obstruct his view of the road and shall be exhibited only when the vehicle is carrying radioactive material.
(d) It shall be in an agreed form and shall state the name, address and telephone number for use in emergencies.
(a) It shall be not less than 12 cm square. All lettering on the notice shall be black, bold and legible. All lettering shall also be embossed or stamped. The capital letters in the word ‘RADIOACTIVE’ shall be not less than 12 mm high and all other capital letters shall be not less than 5 mm high.
(b) It shall be fireproof to the extent that the words on the notice shall remain legible after exposure to a fire involving the vehicle.
(c) It shall be securely posted in the vehicle in a position where it is plainly visible to the driver, but does not obstruct his view of the road and shall be exhibited only when the vehicle is carrying radioactive material.
(d) It shall be in an agreed form and shall state the name, address and telephone number for use in emergencies.
— derogation 2-89: crossing the public highway (chemicals in packages);
— derogation 4-97: distance of 2 km (ingots of pig-iron at a temperature of 600oC);
— derogation 2-2000: distance approximately 500 m (IBC, PG II, III Classes 3, 5.1, 6.1, 8 and 9).
(1) training packages;
(2) training tank;
(3) special training Cl 1;
(4) special training Cl 7.
(a) for the consignee in case of local distribution (except for full load and for transport with certain routings);
(b) for the amount and types of packagings, if 1.1.3.6. is not applied and if the vehicle is in conformity with all provisions of Annex A and B;
(c) for empty uncleaned tanks the transport document of the last load is sufficient.
1. ADR paragraphs for inspection and tests, 6.8.2.4.2, 6.8.2.4.3, 6.8.2.4.4, 6.8.2.4.5, (ADR 1999: 211.151, 211.152, 211.153, 211.154).
2. Minimum shell thickness 3 mm for tanks with shells compartment capacity up to 3 500 lt and at least 4 mm thickness of mild steel for tanks with compartments with capacity up to 6 000 litres, regardless the type or thickness of the partitions.
3. If the used material is aluminium or other metal, tanks should fulfil the requirements for thickness and other technical specifications that derive from technical drawings approved from the local authority of the country where were previously registered. In case of absence of technical drawings, tanks should fulfil the requirements of paragraph 6.8.2.1.17. (211.127).
4. Tanks should fulfil marginal-paragraphs 211.128, 6.8.2.1.28. (211.129), paragraph 6.8.2.2. with sub-paragraphs 6.8.2.2.1. and 6.8.2.2.2. (211.130, 211.131).
a. 1.1.3.6;
b. 3.3;
c. 4.1.4; 4.1.6; 4.1.8; 4.1.10;
d. 5.2.2; 5.4.0; 5.4.1; 5.4.3;
e. 7.5.4; 7.5.7;
f. 8.1.2.1. subsections a) and b); 8.1.5. subsection c); 8.3.6.
10a. The attendant's certificate of professional competence and the note referred to in Article 16(1)(b) are both on board the vehicle;
16b. The vehicle attendant holds the qualification ‘transport of hazardous waste’ issued by the CCV (Drivers' Certification Board).
1. The domestic hazardous waste is to be presented only in a hermetically sealed packaging that is appropriate for the substance in question, and:(a)for objects coming under category 6.2: a packaging guaranteed not to cause injury upon presentation;(b)for domestic hazardous waste of industrial origin: a box having a capacity of not more than 60 litres, in which the waste substances are separated according to danger category (kga-box). (a) for objects coming under category 6.2: a packaging guaranteed not to cause injury upon presentation; (b) for domestic hazardous waste of industrial origin: a box having a capacity of not more than 60 litres, in which the waste substances are separated according to danger category (kga-box).
(a) for objects coming under category 6.2: a packaging guaranteed not to cause injury upon presentation;
(b) for domestic hazardous waste of industrial origin: a box having a capacity of not more than 60 litres, in which the waste substances are separated according to danger category (kga-box).
(a) for objects coming under category 6.2: a packaging guaranteed not to cause injury upon presentation;
(b) for domestic hazardous waste of industrial origin: a box having a capacity of not more than 60 litres, in which the waste substances are separated according to danger category (kga-box).
2. The packaging is free, on the outside, from domestic hazardous waste.
3. The name of the substance is indicated on the packaging.
4. For each collection, only one box within the meaning of point 1, subsection b, will be accepted.
1. The vehicle is fitted with units which, during transport:(a)are protected against accidental displacement; and(b)are sealed with a lid and protected against accidental opening. (a) are protected against accidental displacement; and (b) are sealed with a lid and protected against accidental opening.
(a) are protected against accidental displacement; and
(b) are sealed with a lid and protected against accidental opening.
(a) are protected against accidental displacement; and
(b) are sealed with a lid and protected against accidental opening.
2. Point 1, subsection b, is not applicable during transit for collection purposes or when the vehicle is stationary on its collection rounds.
3. A sufficiently large clearance zone should be set aside in the vehicle so as to enable the domestic hazardous waste to be sorted and deposited in the different units.
1. Domestic hazardous waste is exclusively transported in elements.
2. There is a separate element for substances and objects in each class.
3. With regard to class 8 substances and objects, there are separate elements for acids, bases and batteries.
4. Spray cans may be placed in closable cardboard boxes provided that these boxes are transported in accordance with Article 9(1).
5. If class 2 fire extinguishers have been collected, they may be placed in the same element as spray cans not packed in cardboard boxes.
6. By derogation from Article 9(1), no lid is required for the transport of batteries, provided that they are placed in the element in such a way that all of the batteries' openings are closed off and face upward.
1. The elements, or boxes destined for transport of spray cans, should be clearly marked as follows:(a)for class 2 sprays collected in cardboard boxes: the word ‘SPUITBUSSEN’ [spray cans];(b)for class 2 fire extinguishers and spray cans: label No 2.2;(c)for class 3 fire extinguishers and spray cans: label No 3;(d)for class 4.1. paint waste: label No 4.1;(e)for class 6.1. noxious substances: label No 6.1;(f)for class 6.2. objects: label No 6.2;(g)for class 8 caustic substances and objects: label No 8; and furthermore:(h)for alkaline substances: the word ‘BASEN’ [bases];(i)for acidic substances: the word ‘ZUREN’ [acids];(j)for batteries: the word ‘ACCU'S’ [batteries]. (a) for class 2 sprays collected in cardboard boxes: the word ‘SPUITBUSSEN’ [spray cans]; (b) for class 2 fire extinguishers and spray cans: label No 2.2; (c) for class 3 fire extinguishers and spray cans: label No 3; (d) for class 4.1. paint waste: label No 4.1; (e) for class 6.1. noxious substances: label No 6.1; (f) for class 6.2. objects: label No 6.2; (g) for class 8 caustic substances and objects: label No 8; and furthermore: (h) for alkaline substances: the word ‘BASEN’ [bases]; (i) for acidic substances: the word ‘ZUREN’ [acids]; (j) for batteries: the word ‘ACCU'S’ [batteries].
(a) for class 2 sprays collected in cardboard boxes: the word ‘SPUITBUSSEN’ [spray cans];
(b) for class 2 fire extinguishers and spray cans: label No 2.2;
(c) for class 3 fire extinguishers and spray cans: label No 3;
(d) for class 4.1. paint waste: label No 4.1;
(e) for class 6.1. noxious substances: label No 6.1;
(f) for class 6.2. objects: label No 6.2;
(g) for class 8 caustic substances and objects: label No 8; and furthermore:
(h) for alkaline substances: the word ‘BASEN’ [bases];
(i) for acidic substances: the word ‘ZUREN’ [acids];
(j) for batteries: the word ‘ACCU'S’ [batteries].
(a) for class 2 sprays collected in cardboard boxes: the word ‘SPUITBUSSEN’ [spray cans];
(b) for class 2 fire extinguishers and spray cans: label No 2.2;
(c) for class 3 fire extinguishers and spray cans: label No 3;
(d) for class 4.1. paint waste: label No 4.1;
(e) for class 6.1. noxious substances: label No 6.1;
(f) for class 6.2. objects: label No 6.2;
(g) for class 8 caustic substances and objects: label No 8; and furthermore:
(h) for alkaline substances: the word ‘BASEN’ [bases];
(i) for acidic substances: the word ‘ZUREN’ [acids];
(j) for batteries: the word ‘ACCU'S’ [batteries].
2. The same labels and texts are visibly displayed on the closable spaces within the vehicle where the elements may be placed.
1. The transport of food for humans and animal feedingstuffs at the same time as domestic hazardous waste is prohibited.
2. The vehicle must be stationary during collection.
3. An amber flashing light must be operated on the vehicle while it is moving or stationary for collection.
4. During collection at a fixed location, indicated for this purpose, the engine must be switched off and, by derogation from point 3, the flashing light may be switched off.
4. ‘No smoking’ notices must be clearly displayed on the sides and at the rear of the vehicle.
(a) at least one stop block for each vehicle with a size appropriate for the vehicle's weight and the diameter of the wheels;
(b) the equipment necessary to carry out the general measures indicated in the safety instructions referred to in 5.4.3, in particular:—two separate upright warning signals (e.g. reflective cones, emergency warning triangles, or flashing amber lights that are independent of the vehicle's electrical installation);—a good quality safety jacket or safety clothing (e.g. as described in European standard EN 471) for every crew member;—a hand-held torch (see also 8.3.4) for every crew member;—protective breathing equipment in accordance with additional requirement S7 (see chapter 8.5) if this additional provision is applicable in accordance with the indication in column 19 of table A of chapter 3.2; — two separate upright warning signals (e.g. reflective cones, emergency warning triangles, or flashing amber lights that are independent of the vehicle's electrical installation); — a good quality safety jacket or safety clothing (e.g. as described in European standard EN 471) for every crew member; — a hand-held torch (see also 8.3.4) for every crew member; — protective breathing equipment in accordance with additional requirement S7 (see chapter 8.5) if this additional provision is applicable in accordance with the indication in column 19 of table A of chapter 3.2;
— two separate upright warning signals (e.g. reflective cones, emergency warning triangles, or flashing amber lights that are independent of the vehicle's electrical installation);
— a good quality safety jacket or safety clothing (e.g. as described in European standard EN 471) for every crew member;
— a hand-held torch (see also 8.3.4) for every crew member;
— protective breathing equipment in accordance with additional requirement S7 (see chapter 8.5) if this additional provision is applicable in accordance with the indication in column 19 of table A of chapter 3.2;
— two separate upright warning signals (e.g. reflective cones, emergency warning triangles, or flashing amber lights that are independent of the vehicle's electrical installation);
— a good quality safety jacket or safety clothing (e.g. as described in European standard EN 471) for every crew member;
— a hand-held torch (see also 8.3.4) for every crew member;
— protective breathing equipment in accordance with additional requirement S7 (see chapter 8.5) if this additional provision is applicable in accordance with the indication in column 19 of table A of chapter 3.2;
(c) the equipment necessary to carry out the additional and special measures as indicated in the written instructions referred to in 5.4.3.
(a) fully sealing safety goggles;
(b) protective breathing mask;
(c) acid-resistant, acid-proof overalls or apron;
(d) synthetic-rubber gloves;
(e) acid-proof, acid-resistant boots or safety shoes; and
(f) an eye rinse bottle with distilled water.
— the dangerous goods declaration is not required,
— older tanks/containers not constructed according to chapter 6.8. but according to older national legislation and fitted on crew wagons may still be used,
— older tankers, not fulfilling the requirements in 6.7. or 6.8, intended for the transport of substances of UN 1268, 1999, 3256 and 3257, with or without road surface coating equipment, may still be used for local transport and in close proximity to road work places,
— certificate of approval for crew wagons and tankers with or without road surface coating equipment are not required.
THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Council Directive 94/55/EC of 21 November 1994 on the approximation of the laws of the Member States with regard to the transport of dangerous goods by road(1), and in particular Article 6(9) thereof,
(1) Pursuant to Article 6(9) of Directive 94/55/EC, Member States must give the Commission an advance notification on their derogations for the first time by 31 December 2002 or until two years after the last date of application of the amended versions of the Annexes to the Directive.
(2) Certain Member States had notified the Commission by 31 December 2002 of their wish to adopt derogations from Directive 94/55/EC. By Decision 2003/635/EC of 20 August 2003 authorising Member States pursuant to Directive 94/55/EC to adopt certain derogations with regard to the transport of dangerous goods by road(2), the Commission authorised the adoption by the Member States of the derogations listed in Annexes I and II to that Decision.
(3) Commission Directive 2003/28/EC(3)amended Annexes A and B to Directive 94/55/EC. By virtue of Directive 2003/28/EC Member States had to bring into force national legislation no later than 1 July 2003, the last date of application referred to in Article 6(9) of Directive 94/55/EC being 30 June 2003.
(4) A few Member States notified their wish to adopt derogations. The Commission has examined the notifications for compliance with the conditions laid down in Article 6(9) of Directive 94/55/EC and has approved them. Those Member States should therefore be authorised to adopt the derogations in question.
(5) By the same occasion, it is considered desirable to assemble all the derogations authorised to date in a single decision. Decision 2003/635/EC should therefore be repealed and replaced.
(6) To make sure that the situation of the derogations is updated regularly, the Commission shall propose a comprehensive update of all existing derogations at least every five years.
(7) The measures provided for in this Decision are in accordance with the opinion of the Committee on the transport of dangerous goods, set up by Article 9 of Directive 94/55/EC,
HAS ADOPTED THIS DECISION:

Article 1
Member States listed in Annex I are authorised to implement the derogations set out in Annex I regarding the transportation by road within their territory of small quantities of certain dangerous goods.
These derogations shall be applied without discrimination.

Article 2
Member States listed in Annex II are authorised to implement the derogations set out in Annex II regarding to local transport limited to their territory.
These derogations shall be applied without discrimination.

Article 3
Decision 2003/635/EC is repealed.
References to the repealed Decision shall be construed as references to this Decision.

Article 4
This Decision is addressed to the Member States.

THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Council Directive 94/55/EC of 21 November 1994 on the approximation of the laws of the Member States with regard to the transport of dangerous goods by road(1), and in particular Article 6(9) thereof,
(1) Pursuant to Article 6(9) of Directive 94/55/EC, Member States must give the Commission an advance notification on their derogations for the first time by 31 December 2002 or until two years after the last date of application of the amended versions of the Annexes to the Directive.
(2) Certain Member States had notified the Commission by 31 December 2002 of their wish to adopt derogations from Directive 94/55/EC. By Decision 2003/635/EC of 20 August 2003 authorising Member States pursuant to Directive 94/55/EC to adopt certain derogations with regard to the transport of dangerous goods by road(2), the Commission authorised the adoption by the Member States of the derogations listed in Annexes I and II to that Decision.
(3) Commission Directive 2003/28/EC(3)amended Annexes A and B to Directive 94/55/EC. By virtue of Directive 2003/28/EC Member States had to bring into force national legislation no later than 1 July 2003, the last date of application referred to in Article 6(9) of Directive 94/55/EC being 30 June 2003.
(4) A few Member States notified their wish to adopt derogations. The Commission has examined the notifications for compliance with the conditions laid down in Article 6(9) of Directive 94/55/EC and has approved them. Those Member States should therefore be authorised to adopt the derogations in question.
(5) By the same occasion, it is considered desirable to assemble all the derogations authorised to date in a single decision. Decision 2003/635/EC should therefore be repealed and replaced.
(6) To make sure that the situation of the derogations is updated regularly, the Commission shall propose a comprehensive update of all existing derogations at least every five years.
(7) The measures provided for in this Decision are in accordance with the opinion of the Committee on the transport of dangerous goods, set up by Article 9 of Directive 94/55/EC,
HAS ADOPTED THIS DECISION:
Member States listed in Annex I are authorised to implement the derogations set out in Annex I regarding the transportation by road within their territory of small quantities of certain dangerous goods.
These derogations shall be applied without discrimination.
Member States listed in Annex II are authorised to implement the derogations set out in Annex II regarding to local transport limited to their territory.
These derogations shall be applied without discrimination.
Decision 2003/635/EC is repealed.
References to the repealed Decision shall be construed as references to this Decision.
This Decision is addressed to the Member States.

BELGIUM

ANNEX IDerogations for Member States on small quantities of certain dangerous goodsRO-SQ 1.1Subject:Class 1 — Small quantities.
Reference to the Annex to Directive94/55/EC(hereinafter referred to as the Directive):1.1.3.6.
Content of the Annex to the Directive:Marginal 1.1.3.6. limits to 20 kg the quantity of mining explosives which can be transported in an ordinary vehicle.
Reference to the national legislation:Royal Decree of 23 September 1958 on explosives, as amended by Royal Decree of 14 May 2000.
Content of the national legislation:Article 111. Operators of depots remote from supply points may be authorised to transport 25 kg of dynamite or powerful explosives and 300 detonators at the most in ordinary motor vehicles, subject to conditions to be set by the explosives service.
RO-SQ 1.2Subject:Transport of uncleaned empty containers having contained products of different classes.
Reference to the Annex to the Directive:5.4.1.1.6.
Reference to the national legislation:Derogation 6-97.
Content of the national legislation:Indication on the transport document ‘uncleaned empty packages having contained products of different classes’.
Comments:Derogation registered by the European Commission as No 21 (under Art. 6.10).
DENMARKRO-SQ 2.1Subject:Road transport of packagings containing wastes or residues of dangerous substances collected from households and certain enterprises for the purpose of disposal.
Reference to the Annex to the Directive:Part 2, 4.1.4, 4.1.10, 5.2, 5.4. and 8.2.
Content of the Annex to the Directive:Principles for classification. Mixed packing provisions. Marking and labelling provisions. Transport document.
Reference to the national legislation:Bekendtgørelse nr. 729 of 15. august 2001 om vejtransport of farligt gods § 4, stk. 3.
Content of the national legislation:Inner packagings containing waste or residues of chemicals collected from households and certain enterprises may be packed together in certain UN-approved outer packagings. The contents of each inner packaging must not exceed 5 kg or 5 litre. Derogations from the provisions concerning classification, marking and labelling, documentation and training.
Comments:It is not possible to carry out an accurate classification and apply all ADR provisions when wastes or residual amounts of chemicals are collected from households and certain enterprises for the purpose of disposal. The waste is typically contained in packagings which have been sold in retail sale.
RO-SQ 2.2Subject:Road transport containing packagings of explosive substances and packagings of detonators on the same vehicle.
Reference to the Annex to the Directive:7.5.2.2.
Content of the Annex to the Directive:Mixed packing provisions.
Reference to the national legislation:Bekendtgørelse nr. 729 of 15. august 2001 om vejtransport of farligt gods § 4, stk. l..
Content of the national legislation:According to § 4, stk. 1, the rules in ADR must be observed when transporting dangerous goods by road.
Comments:There is a practical need for being able to pack explosive substances together with detonators the same vehicle when transporting these goods from where they are stored and to the workplace and back again.
When the Danish legislation concerning transport of dangerous goods is amended the Danish authorities will allow such transports on the following conditions:

(1) | Not more than 25 kg explosive substances under group D are being transported.
(2) | Not more than 200 pieces of detonators under group B are being transported.
(3) | Detonators and explosive substances must be packed separately in UN-certified packaging in accordance with the rules in Directive 2000/61/EC amending Directive 94/55/EC.
(4) | The distance between packaging that contains detonators and packaging that contains explosive substances must be at least 1 meter. This distance has to be observed even after a sudden application of the brakes. Packaging containing explosive substances and packaging containing detonators must be placed in a way that makes it possible quickly to remove them from the vehicle.
(5) | All other rules concerning transport of dangerous goods by road must be observed.GERMANYRO-SQ 3.1Subject:Mixed packing and mixed loading of car parts with classification 1.4G together with certain dangerous goods (n4).
Reference to the Annex to the Directive:4.1.10. and 7.5.2.1.
Content of the Annex to the Directive:Provisions on mixed packing and mixed loading.
Reference to the national legislation:Gefahrgut-Ausnahmeverordnung – GGAV 2002 vom 6.11.2002 (BGBl. I S. 4350), geändert durch Artikel 2 der Verordnung vom 28.4.2003 (BGBl. I S. 595); Ausnahme 28.
Content of the national legislation:UN 0431 and UN 0503 may be loaded together with certain dangerous goods (products related to car manufacturing) in certain amounts, listed in the exemption. The value 1 000 (comparable with 1.1.3.6.4) shall not be exceeded.
Comments:The exemption is needed to provide fast delivery of safety car parts depending on the local demand. Due to the wide variety of the product range storage of these products by local garages is not common.
RO-SQ 3.2Subject:Exemption from requirement to carry a transport document and a shippers declaration for certain quantities of dangerous goods as defined in 1.1.3.6. (n1).
Reference to the Annex to the Directive:5.4.1.1.1. and 5.4.1.1.6.
Content of the Annex to the Directive:Contents of the transport document.
Reference to the national legislation:Gefahrgut-Ausnahmeverordnung – GGAV 2002 vom 6.11.2002 (BGBl. I S. 4350), geändert durch Artikel 2 der Verordnung vom 28.4.2003 (BGBl. I S. 595); Ausnahme 18.
Content of the national legislation:For all classes except class 7: no transport document needed, if the quantity of the goods transported is not exceeding the quantities given in 1.1.3.6.
Comments:The information provided by the marking and labelling of packages is considered sufficient for national transports, as a transport document is not always appropriate where local distribution is involved.
Derogation is registered by the European Commission as No 22 (under Article 6.10)
RO-SQ 3.3. (Revoked)
RO-SQ 3.4Subject:Transportation of measurement standards and fuel pumps (empty, non-cleaned).
Reference to the Annex to the Directive:Provisions for UN numbers 1202, 1203 und 1223.
Content of the Annex to the Directive:Packaging, marking, documents, transport and handling instructions, instructions for vehicle crews.
Reference to the national legislation:Gefahrgut-Ausnahmeverordnung – GGAV 2002 vom 6.11.2002 (BGBl. I S. 4350), geändert durch Artikel 2 der Verordnung vom 28.4.2003 (BGBl. I S. 595); Ausnahme 24.
Content of the national legislation:Specification of applicable regulations and ancillary provisions for applying the derogation; up to 1 000 l: comparable with empty, non-cleaned packagings; above 1 000 l: Compliance with certain regulations for tanks; transportation empty and non-cleaned only.
Comments:List No 7, 38, 38a.
RO-SQ 3.5Subject:Exemption of small quantities of certain goods for private use.
Reference to the Annex to the Directive:Table in Chapter 3.2. for certain UN numbers in Classes 1 to 9.
Content of the Annex to the Directive:Transport authorisation and provisions.
Reference to the national legislation:Gefahrgut-Ausnahmeverordnung – GGAV 2002 vom 6.11.2002 (BGBl. I S. 4350), geändert durch Artikel 2 der Verordnung vom 28.4.2003 (BGBl. I S. 595); Ausnahme 3.
Content of the national legislation:Classes 1 to 9; Exemption for very small quantities of various goods in packagings and quantities for private use; a maximum of 50 kg per transport unit; application of the general packing requirements for internal packaging.
Comments:Derogation limited to 31.12.2004.
List No 14*.
RO-SQ 3.6Subject:Combined packaging authorisation.
Reference to the Annex to the Directive:4.1.10.4. MP2.
Content of the Annex to the Directive:Prohibition of combined packaging.
Reference to the national legislation:Gefahrgut-Ausnahmeverordnung – GGAV 2002 vom 6.11.2002 (BGBl. I S. 4350), geändert durch Artikel 2 der Verordnung vom 28.4.2003 (BGBl. I S. 595); Ausnahme 21.
Content of the national legislation:Classes 1.4S, 2, 3 and 6.1; authorisation of combined packaging of objects in Class 1.4S (cartridges for small weapons), aerosols (Class 2) and cleaning and treatment materials in Classes 3 and 6.1. (UN numbers listed) as sets to be sold in combined packaging in packaging group II and in small quantities.
Comments:List No 30*, 30a, 30b, 30c, 30d, 30e, 30f, 30g.
FRANCERO-SQ 6.1Subject:Transport of portable and mobile gamma radiography equipment (18).
Reference to the Annex to the Directive:Annexes A et B.
Content of the Annex to the Directive: –
Reference to the national legislation:Arrêté du 1erjuin 2001 relatif au transport de marchandises dangereuses par route (Decree of 1 June 2001 on the transport of hazardous goods by road, ‘ADR-Decree’) – Article 28.
Content of the national legislation:The transport of gamma radiography equipment by users in special vehicles is exempted but subject to specific rules.
RO-SQ 6.2Subject:Transport of waste arising from care activities involving infectious risks and treated as anatomical parts covered by UN 3291 with a mass less than or equal to 15 kg.
Reference to the Annex to the Directive:Annexes A et B.
Reference to the national legislation:Arrêté du 1erjuin 2001 relatif au transport de marchandises dangereuses par route (Decree of 1 June 2001 on the transport of hazardous goods by road, ‘ADR-Decree’) – Article 12.
Content of the national legislation:Exemption from the requirements of the ADR for the transport of waste arising from care activities involving infectious risks and treated as anatomical parts covered by UN 3291 with a mass less than or equal to 15 kg.
RO-SQ 6.3Subject:Transport of hazardous substances in public passenger transport vehicles (18).
Reference to the Annex to the Directive:8.3.1.
Content of the Annex to the Directive:Transport of passengers and hazardous substances.
Reference to the national legislation:Arrêté du 1erjuin 2001 relatif au transport de marchandises dangereuses par route (Decree of 1 June 2001 on the transport of hazardous goods by road, ‘ADR-Decree’) – Article 21.
Content of the national legislation:Transport of hazardous substances authorised in public transport vehicles as hand luggage: only the provisions relating to the packaging, marking and labelling of parcels set out in 4.1, 5.2. and 3.4. apply.
Comments:In hand luggage it is allowed to have only dangerous goods for personal or own professional use. Portable gas receptacles allowed for patients with respiratory problems in the necessary amount for one journey.
RO-SQ 6.4Subject:Own-account transport of small quantities of hazardous materials (18).
Reference to the Annex to the Directive:5.4.1.
Content of the Annex to the Directive:Obligation to have a transport document.
Reference to the national legislation:Arrêté du 1erjuin 2001 relatif au transport de marchandises dangereuses par route (Decree of 1 June 2001 on the transport of hazardous goods by road, ‘ADR-Decree’) – Article 23-2.
Content of the national legislation:Own-account transport of small quantities of hazardous materials not exceeding the limits set in 1.1.3.6. is not subject to the obligation to have a transport document provided for in 5.4.1.
IRELANDRO-SQ 7.2Subject:Exemption from the requirement of 5.4.0. of the ADR for a transport document for the carriage of pesticides of ADR Class 3, listed under 2.2.3.3. as FT2 pesticides (f.p. < 23oC) and ADR Class 6.1, listed under 2.2.61.3. as T6 pesticides, liquid (flash point not less than 23oC), where the quantities of dangerous goods being carried do not exceed the quantities set out in 1.1.3.6. of the ADR.
Reference to the Annex to the Directive:5.4.
Content of the Annex to the Directive:Requirement for transport document.
Reference to the national legislation:Regulation 82(9) of the Carriage of Dangerous Goods by Road Regulations 2004.
Content of the national legislation:Transport document is not required for the carriage of those pesticides of ADR Classes 3 and 6.1, where the quantity of dangerous goods being carried does not exceed the quantities set out in 1.1.3.6. of the ADR.
Comments:Unnecessary, onerous requirement for local transport and delivery of those pesticides.
RO-SQ 7.4Subject:Exemption from requirement from some of the provisions of the ADR on the packaging, marking and labelling of the carriage of small quantities (below the limits in 1.1.3.6) of time expired pyrotechnic articles of classification codes 1.3G, 1.4G and 1.4S of Class 1 of the ADR, bearing the respective substance identification numbers UN0092, UN0093, UN0403 or UN0404, to the nearest military barracks for disposal.
Reference to the Annex to the Directive:1.1.3.6, 4.1, 5.2. and 6.1.
Content of the Annex to the Directive:Disposal of out of date pyrotechnics.
Reference to the national legislation:Regulation 82(10) of the Carriage of Dangerous Goods by Road Regulations 2004.
Content of the national legislation:The provisions of the ADR on the packaging, marking and labelling of the carriage of expired pyrotechnic articles bearing the respective UN numbers UN 0092, UN 0093, UN 0403, UN 0404 to the nearest military barracks do not apply provided the general packaging provisions of the ADR are complied with and additional information is included in the transport document. It applies only to the local transport, to the nearest military barracks, of small quantities of these time expired pyrotechnics for safe disposal.
Comments:The carriage of small quantities of ‘time expired’ marine emergency flares, especially from pleasure boat owners and ships chandlers, to military barracks for their safe disposal has created difficulties; particularly in relation to packaging requirements. The derogation is for small quantities (below those specified in 1.1.3.6) on local transport.
RO-SQ 7.5Subject:Exemption from the requirements of Chapters 6.7. and 6.8, in relation to the transport by road of nominally empty uncleaned storage tanks (for storage at fixed locations) for the purpose of cleaning, repair, testing or scrapping.
Reference to the Annex to the Directive:6.7. and 6.8.
Content of the Annex to the Directive:Requirements for the design, construction, inspection and testing of tanks.
Reference to the national legislation:Proposed amendment to the Carriage of Dangerous Goods by Road Regulations, 2004.
Content of the national legislation:[Proposed] Exemption from the requirements of Chapters 6.7. and 6.8. of the ADR for the carriage by road of nominally empty uncleaned storage tanks (for storage at fixed premises) for the purpose of cleaning, repair, testing or scrapping; provided (a) as much of the pipe work which was connected to the tank as it was reasonably practicable to remove from it has been removed; (b) a suitable pressure relief valve, which shall remain operational during the carriage, is fitted to the tank; and (c) subject to (b) above all openings in the tank and in any pipe work attached thereto have been sealed to prevent the escape of any dangerous goods; insofar as it is reasonably practicable to do so.
Comments:These tanks are used for storage of substances at fixed premises and not for the transport of goods. They would contain very small quantities of dangerous goods while they (the tanks) were being transported to different premises for cleaning, repairs, etc.
Previously under Article 6.10.
RO-SQ 7.6Subject:Exemption from the requirements of Chapters 5.3, 5.4, Part 7 and Annex B of the ADR, in relation to the carriage of gas cylinders of dispensing agents (for beverages) where they are carried on the same vehicle as the beverages (for which they are to be used).
Reference to the Annex to the Directive:Chapters 5.3, 5.4, Part 7 and Annex B.
Content of the Annex to the Directive:The marking of the vehicles, the documentation to be carried and the provisions concerning transport equipment and transport operations.
Reference to the national legislation:Proposed amendment to the Carriage of Dangerous Goods by Road Regulations, 2004.
Content of the national legislation:[Proposed] Exemption from the requirements of Chapters 5.3, 5.4, Part 7 and Annex B of the ADR for cylinders of gases, used as dispensing agents for beverages, where these cylinders of gases are carried on the same vehicle as the beverages (for which they are to be used).
Comments:The main activity consists of the distribution of packages of beverages, that are not substances of ADR, together with small quantities of small cylinders of associated dispensing gases.
Previously under Article 6.10.
RO-SQ 7.7Subject:Exemption, for national transport within Ireland, from the construction and testing requirements for receptacles, and their use provisions, contained in Chapters 6.2. and 4.1. of the ADR for cylinders and pressure drums of gases of Class 2; that have undergone a multimodal transport journey, including maritime carriage, where (i) these cylinders and pressure drums are constructed, tested and used in accordance with the IMDG Code, (ii) these cylinders and pressure drums are not refilled in Ireland but returned nominally empty to the country of origin of the multimodal transport journey, and (iii) these cylinders and pressure drums are distributed locally in small quantities.
Reference to the Annex to the Directive:1.1.4.2, 4.1. and 6.2.
Content of the Annex to the Directive:Provisions relating to multimodal transport journey, including maritime carriage, use of cylinders and pressure drums for gases of ADR Class2, and construction and testing of these cylinders and pressure drums for gases of ADR Class 2.
Reference to the national legislation:Proposed amendment to the Carriage of Dangerous Goods by Road Regulations, 2004.
Content of the national legislation:[Proposed] The provisions of Chapters 4.1. and 6.2. do not apply to cylinders and pressure drums of gases of Class 2 provided (i) these cylinders and pressure drums are constructed and tested in accordance with the IMDG Code, (ii) these cylinders and pressure drums are used in accordance with the IMDG Code, (iii) these cylinders and pressure drums were transported to the consignor by means of a multimodal transport, including maritime carriage, (iv) the transport of these cylinders and pressure drums to the final user consists only of a single transport journey, completed within the same day, from the consignee of the multimodal transport [referred to in subparagraph (iii) above], (v) these cylinders and pressure drums are not refilled within the State and returned nominally empty to the country of origin of the multimodal transport [referred to in subparagraph (iii) above], and (vi) these cylinders and pressure drums are distributed locally within the State in small quantities.
Comments:The gases contained in these cylinders and pressure drums are of a specification, required by the final users, which results in the need to import them from outside the ADR area. Following use, these nominally empty cylinders and pressure drums are required to be returned to the country of origin, for refilling with the specially specified gases – they are not to be refilled within Ireland or indeed within any part of the ADR area. Though not in compliance with ADR, they are in compliance with and accepted for the IMDG Code. The multimodal transport, beginning from outside the ADR area, is intended to finish at the importers premises, from where it is intended to distribute these cylinders and pressure drums to the final user locally within Ireland in small quantities. This carriage, within Ireland, would come within the amended Art 6(9) of amended Directive 94/55/EC.
FINLANDRO-SQ 13.1Subject:Transport of dangerous goods in certain amounts in private cars and buses.
Reference to the Annex to the Directive:4.1, 5.4.
Content of the Annex to the Directive:Packaging provisions, documentation.
Reference to the national legislation:Liikenne- ja viestintäministeriön asetus vaarallisten aineiden kuljetuksesta tiellä (277/2002; 313/2003).
Content of the national legislation:Transport of dangerous goods in certain amounts under that of 1.1.3.6. with a maximum net mass of not more than 200 kg in private cars and buses is allowed without using the transport document and without fulfilling all the packaging requirements.
RO-SQ 13.2Subject:Description of empty tanks in the transport document.
Reference to the Annex to the Directive:5.4.1.1.6.
Content of the Annex to the Directive:Special provisions for empty uncleaned packagings, vehicles, containers, tanks, battery-vehicles and MEGCs.
Reference to the national legislation:Liikenne- ja viestintäministeriön asetus vaarallisten aineiden kuljetuksesta tiellä (277/2002; 313/2003).
Content of the national legislation:In the case of empty, uncleaned tank vehicles in which two or more substances with UN numbers 1202, 1203 and 1223 have been carried, the description in the transport documents may be completed by words ‘Last load’ together with the name of the product having the lowest flashpoint; ‘Empty tank vehicle, 3, last load: UN 1203 Motor spirit, II’.
RO-SQ 13.3Subject:Labelling and marking of the transport unit for explosives.
Reference to the Annex to the Directive:5.3.2.1.1.
Content of the Annex to the Directive:General orange-coloured plate marking provisions.
Reference to the national legislation:Liikenne- ja viestintäministeriön asetus vaarallisten aineiden kuljetuksesta tiellä (277/2002; 313/2003).
Content of the national legislation:Transport units transporting (normally in vans) small amounts of explosives (maximum 1 000 kg (net)) to quarries and working sites may be labelled at the front and at the rear, using the placard in model No 1.
RO-SQ 13.4Subject:Adoption of RO-SQ 6.2.
Reference to the national legislation:To be specified in forthcoming Regulations.
RO-SQ 13.5Subject:Adoption of RO-SQ 6.4.
Reference to the national legislation:To be specified in forthcoming Regulations.
THE UNITED KINGDOMRO-SQ 15.1Subject:Carriage of certain low-hazard radioactives such as clocks, watches, smoke detectors, compass dials (E1).
Reference to the Annex to the Directive:Most requirements of ADR.
Content of the Annex to the Directive:Requirements concerning the carriage of Class 7 material.
Reference to the national legislation:Radioactive Material (Road Transport) (Great Britain) Regulations 1996, Regulation 3(2)(f), (g) and (h).
Content of the national legislation:Total exemption from the provisions of the national regulations for certain commercial products containing limited quantities of radioactive material.
Comments:This derogation is a short-term measure, which will no longer be required when similar amendments to the IAEA regulations are incorporated into ADR
RO-SQ 15.2Subject:Exemption from requirement to carry a transport document for certain quantities of dangerous goods as defined in 1.1.3.6. (E2).
Reference to the Annex to the Directive:1.1.3.6.2. and 1.1.3.6.3.
Content of the Annex to the Directive:Exemptions from certain requirements for certain quantities per transport unit.
Reference to the national legislation:Carriage of Dangerous Goods by Road Regulations 1996, Regulation 3 and Regulation 13 and Schedule 2(8).
Content of the national legislation:Transport document is not required for limited quantities except where these form part of a larger load.
Comments:This exemption is suited to national transport, where a transport document is not always appropriate where local distribution is involved .
RO-SQ 15.3Subject:Carriage of light gauge metal cylinders for use in hot-air balloons between the filling site and the launch/landing site (E3).
Reference to the Annex to the Directive:6.2.
Content of the Annex to the Directive:Requirements for construction and testing of gas receptacles.
Reference to the national legislation:To be specified in forthcoming Regulations.
Content of the national legislation:See above.
Comments:Gas cylinders used for hot-air balloons are designed to be as light-weight as possible, which precludes their meeting the normal requirements for gas cylinders. The average balloon cylinder has a water capacity of 70 litres, and the largest does not exceed 90 litres. Not more than five cylinders are carried on the vehicle at any one time.
RO-SQ 15.4Subject:Exemption from requirement of fire-fighting equipment for vehicles carrying low-level radioactive material (E4).
Reference to the Annex to the Directive:8.1.4.
Content of the Annex to the Directive:Requirement for vehicles to carry fire-fighting appliances.
Reference to the national legislation:Radioactive Material (Road Transport) (Great Britain) 1996, Regulation 34(4) and (5).
Content of the national legislation:Regulation 34(4) removes requirement for carrying fire extinguishers when carrying only excepted packages (UN 2908, 2909, 2910 and 2911).
Reg. 34(5) restricts the requirement where only a small numbers of packages are carried.
Comments:Carriage of fire-fighting equipment is in practice irrelevant to transport of UN 2908, 2909, 2910, UN 2911, which may often be carried in small vehicles.
RO-SQ 15.5Subject:Distribution of goods in inner packagings to retailers or users (excluding those of classes 1 and 7) from local distribution depots to retailers or users and from retailers to end users (N1).
Reference to the Annex to the Directive:6.1.
Content of the Annex to the Directive:Requirements for the construction and testing of packagings.
Reference to the national legislation:Carriage of Dangerous Goods (Classification, Packaging & Labelling) and Use of Transportable Pressure Receptacles Regulations 1996, Regulations 6(1), 6(3) and 8(5) and Schedule 3.
Content of the national legislation:Packagings are not required to have been allocated an RID/ADR or UN mark or to be otherwise marked if they contain goods as set out in Schedule 3.
Comments:ADR requirements are inappropriate for the final stages of carriage from a distribution depot to a retailer or user or from a retailer to an end user. The purpose of this derogation is to allow the inner receptacles of goods for retail distribution to be carried on the final leg of a local distribution journey without an outer packaging.
RO-SQ 15.6Subject:Movement of nominally empty fixed tanks not intended as transport equipment (N2).
Reference to the Annex to the Directive:Parts 5 and 7 to 9.
Content of the Annex to the Directive:Requirements concerning consignment procedures, carriage, operation and vehicles.
Reference to the national legislation:To be specified in forthcoming Regulations.
Content of the national legislation:See above.
Comments:Movement of such fixed tanks is not carriage of dangerous goods in the normal sense, and ADR provisions cannot in practice be applied. As the tanks are ‘nominally empty’, the amount of dangerous goods actually contained in them is by definition extremely small.
RO-SQ 15.7Subject:To allow different ‘maximum total quantity per transport uni’ for Class 1 goods in categories 1 and 2 of table in 1.1.3.6.3. (N10).
Reference to the Annex to the Directive:1.1.3.6.3. and 1.1.3.6.4
Content of the Annex to the Directive:Exemptions related to quantities carried per transport unit.
Reference to the national legislation:Carriage of Explosives by Road Regulations 1996, Regulation 13 and Schedule 5; Regulation 14 and Schedule 4.
Content of the national legislation:Lays down rules regarding exemptions for limited quantities and mixed loading of explosives.
Comments:To allow different quantity limits for Class 1 goods, viz ‘50’ for Category 1 and ‘500’ for category 2. For the purpose of calculating mixed loads, the multiplication factors to read ‘20’ for Transport Category 2 and ‘2’ for Transport Category 3.
Previously a derogation under Article 6.10.
RO-SQ 15.8Subject:Increase of maximum net mass of explosive articles permissible in EX/II vehicles (N13).
Reference to the Annex to the Directive:7.5.5.2.
Content of the Annex to the Directive:Limitations on quantities carried for explosive substances and articles.
Reference to the national legislation:Carriage of Explosives by Road Regulations 1996, Regulation13, Schedule 3.
Content of the national legislation:Limitations on quantities carried for explosive substances and articles.
Comments:United Kingdom Regulations allow a maximum net mass of 5 000 kg in Type II vehicles for Compatibility Groups 1.1C, 1.1D, 1.1E and 1.1J.
Many articles of Class 1.1C, 1,1D, 1.1E and 1.1J being moved in Europe are large or bulky and exceed about 2,5. m in length. They are primarily explosive articles for military use. The limitations on the construction for EX/III vehicles (which are required to be closed vehicles) make it very difficult to load and unload such articles. Some articles would require specialist loading and unloading equipment at both ends of the journey. In practice, this equipment rarely exists. There are few EX/III vehicles in use in the United Kingdom and it would be extremely onerous on industry to require further specialist EX/III vehicles to be constructed to carry this type of explosive.
In the United Kingdom military explosives are mostly carried by commercial carriers and are thus unable to take advantages of the exemption for military vehicles in the Framework Directive. To overcome this problem, the United Kingdom has always permitted the carriage of up to 5 000 kg of such articles on EX/II vehicles. The present limit is not always sufficient because an article may contain more than 1 000 kg of explosive.
Since 1950 there have been only two incidents (both in the 1950s) involving blasting explosives with a weight above 5 000 kg. The incidents were caused by a tyre fire and a hot exhaust system setting fire to the sheeting. The fires could have occurred with a smaller load. There were no fatalities or injuries.
There is empirical evidence to suggest that correctly packaged explosive articles would be unlikely to be initiated due to impact, e.g. from vehicle collisions. Evidence from military reports and from trials data on missile impact tests shows that it needs an impact velocity in excess of that created by the 12-metre drop test to bring about initiation of cartridges.
Present safety standards would not be affected.
RO-SQ 15.9Subject:Exemption from supervision requirements for small quantities of certain Class 1 goods (N12).
Reference to the Annex to the Directive:8.4. and 8.5. S1(6).
Content of the Annex to the Directive:Supervision requirements for vehicles carrying certain quantities of dangerous goods.
Reference to the national legislation:Carriage of Dangerous Goods by Road Regulations 1996, Regulation 24.
Content of the national legislation:Provides for safe parking and supervision facilities but does not require that certain Class 1 loads be supervised at all times as required in ADR Chapter 8.5. S1(6).
Comments:ADR supervision requirements are not always feasible in a national context.
RO-SQ 15.10Subject:Easing of restrictions on transporting mixed loads of explosives, and explosives with other dangerous goods, in wagons, vehicles and containers (N4/5/6).
Reference to the Annex to the Directive:7.5.2.1. and 7.5.2.2.
Content of the Annex to the Directive:Restrictions on certain types of mixed loading.
Reference to the national legislation:Carriage of Dangerous Goods by Road Regulations 1996, Regulation18.
Content of the national legislation:National legislation is less restrictive regarding mixed loading of explosives, providing such carriage can be accomplished without risk.
Comments:The United Kingdom wishes to permit some variations on the mixing rules for explosives with other explosives and for explosives with other dangerous goods. Any variation will have a quantity limitation on one or more constituent parts of the load and would only be permitted provided that ‘all reasonably practicable measures have been taken to prevent the explosives being brought into contact with, or otherwise endangering or being endangered by, any such goods.’
Examples of variations the United Kingdom may want to permit are:

1. | Explosives allocated on classification to UN Numbers 0029, 0030, 0042, 0065, 0081, 0082, 0104, 0241, 0255, 0267, 0283, 0289, 0290, 0331, 0332, 0360, or 0361 may be carried in the same vehicle with the dangerous goods allocated on classification the UN Number 1942. The quantity of UN 1942 permitted to be carried shall be limited by deeming it to be an explosive of 1.1D;
2. | Explosives allocated on classification to UN Number 0191, 0197, 0312, 0336, 0403, 0431, or 0453 may be carried in the same vehicle with dangerous goods (except flammable gases, infectious substances and toxic substances) in transport category 2 or dangerous goods in transport category 3, or any combination of them, provided the total mass or volume of dangerous goods in transport category 2 does not exceed 500 kg or l and the total net mass of such explosives does not exceed 500 kg;
3. | Explosives of 1,4G may be carried with flammable liquids and flammable gases in transport category 2 or non-flammable, non-toxic gases in transport category 3, or in any combination of them in the same vehicle, provided the total mass or volume of dangerous goods when added together does not exceed 200 kg or litres and the total net mass of explosives does not exceed 20 kg.
4. | Explosive articles allocated on classification to UN Numbers 0106, 0107 or 0257 may be carried with explosive articles in Compatibility Group D, E or F for which they are components. The total quantity of explosives of UN Numbers 0106, 0107 or 0257 shall not exceed 20 kg.RO-SQ 15.11Subject:Alternative to display of orange plates for small consignments of radioactive material in small vehicles.
Reference to the Annex to the Directive:5.3.2.
Content of the Annex to the Directive:Requirement for orange plates to be displayed on small vehicles carrying radioactive material.
Reference to the national legislation:The Radioactive Material (Road Transport) Regulations 2002 Regulation 5 (4) (d).
Content of the national legislation:Permits any derogation approved under this process. The derogation requested is:

1. | Vehicles must either:(a)be placarded according to the applicable provisions of ADR paragraph 5.3.2; or(b)in the case of a vehicles of less than 3 500 kg weight, carrying less than 10 packages containing non-fissile or fissile excepted radioactive material and where the sum of the transport indexes of these packages do not exceed 3, may alternatively carry a notice conforming to the requirements of paragraph 2. | (a) | be placarded according to the applicable provisions of ADR paragraph 5.3.2; or | (b) | in the case of a vehicles of less than 3 500 kg weight, carrying less than 10 packages containing non-fissile or fissile excepted radioactive material and where the sum of the transport indexes of these packages do not exceed 3, may alternatively carry a notice conforming to the requirements of paragraph 2.
(a) | be placarded according to the applicable provisions of ADR paragraph 5.3.2; or
(b) | in the case of a vehicles of less than 3 500 kg weight, carrying less than 10 packages containing non-fissile or fissile excepted radioactive material and where the sum of the transport indexes of these packages do not exceed 3, may alternatively carry a notice conforming to the requirements of paragraph 2.
2. | For the purposes of paragraph 1, the notice to be displayed in a vehicle while it is carrying radioactive material shall conform to the following:(a)It shall be not less than 12 cm square. All lettering on the notice shall be black, bold and legible. All lettering shall also be embossed or stamped. The capital letters in the word ‘RADIOACTIVE’ shall be not less than 12 mm high and all other capital letters shall be not less than 5 mm high.(b)It shall be fireproof to the extent that the words on the notice shall remain legible after exposure to a fire involving the vehicle.(c)It shall be securely posted in the vehicle in a position where it is plainly visible to the driver, but does not obstruct his view of the road and shall be exhibited only when the vehicle is carrying radioactive material.(d)It shall be in an agreed form and shall state the name, address and telephone number for use in emergencies. | (a) | It shall be not less than 12 cm square. All lettering on the notice shall be black, bold and legible. All lettering shall also be embossed or stamped. The capital letters in the word ‘RADIOACTIVE’ shall be not less than 12 mm high and all other capital letters shall be not less than 5 mm high. | (b) | It shall be fireproof to the extent that the words on the notice shall remain legible after exposure to a fire involving the vehicle. | (c) | It shall be securely posted in the vehicle in a position where it is plainly visible to the driver, but does not obstruct his view of the road and shall be exhibited only when the vehicle is carrying radioactive material. | (d) | It shall be in an agreed form and shall state the name, address and telephone number for use in emergencies.
(a) | It shall be not less than 12 cm square. All lettering on the notice shall be black, bold and legible. All lettering shall also be embossed or stamped. The capital letters in the word ‘RADIOACTIVE’ shall be not less than 12 mm high and all other capital letters shall be not less than 5 mm high.
(b) | It shall be fireproof to the extent that the words on the notice shall remain legible after exposure to a fire involving the vehicle.
(c) | It shall be securely posted in the vehicle in a position where it is plainly visible to the driver, but does not obstruct his view of the road and shall be exhibited only when the vehicle is carrying radioactive material.
(d) | It shall be in an agreed form and shall state the name, address and telephone number for use in emergencies.Comments:The derogation is required for limited movements of small quantities of radioactive material, primarily single patient doses of radioactive materials between local hospital facilities, where small vehicles are used and the ability to affix even small orange placards is limited. Experience has shown that for these vehicles the fixing of orange placards is problematic and they are difficult to retain under normal conditions of transport. The vehicles will be marked with placards identifying the contents in accordance with ADR 5.3.1.5.2. (and normally 5.3.1.7.4) clearly identifying the hazard. In addition, a fireproof notice carrying relevant emergency information will be attached in a clearly visible location. In practice, more safety information will be available than under the requirements of ADR 5.3.2.

BELGIUM

ANNEX IIDerogations for Member States on local transport limited to their territoryRO-LT 1.1Subject:Transport in close proximity of industrial sites including transport on public road.
Reference to the Annex to Directive94/55/EC(hereinafter referred to as the Directive):Annexes A and B.
Content of the Annex to the Directive:Annexes A and B.
Reference to the national legislation:Derogations 2-89, 4-97 and 2-2000.
Content of the national legislation:The derogations concern the documentation, labelling and marking of packages and the driver’s certificate.
Comments:Dangerous goods are transferred between premises

— | derogation 2-89: crossing the public highway (chemicals in packages);
— | derogation 4-97: distance of 2 km (ingots of pig-iron at a temperature of 600oC);
— | derogation 2-2000: distance approximately 500 m (IBC, PG II, III Classes 3, 5.1, 6.1, 8 and 9).RO-LT 1.2Subject:Movement of storage tanks not intended as transport equipment.
Reference to the Annex to the Directive:1.1.3.2.(f).
Reference to the national legislation:exemption 6-82, 2-85.
Content of the national legislation:Movements of nominally storage tanks for cleaning/repair purposes allowed.
Comments:Derogation registered by the European Commission as No 7 (under Article 6.10).
RO-LT 1.3Subject:Training of drivers.
Local transport of UN 1202, 1203 and 1223 in packages and in tanks (in Belgium radius of 75 km from the location of the registered office).
Reference to the Annex to the Directive:8.2
Content of the Annex to the Directive:
Structure of the training:

(1) | training packages;
(2) | training tank;
(3) | special training Cl 1;
(4) | special training Cl 7.Reference to the national legislation:To be specified in forthcoming regulation.
Content of the national legislation:Definitions — certificate — issue — duplicates — validity and extension — organisation of courses and examination — derogations — penalties — final provisions.
Comments:It is proposed to give an initial course followed by an examination limited to the transport of UN 1202, 1203 and 1223 in packages and in tanks in a radius of 75 km from the location of the registered office — the length of training must meet the requirements of the ADR – after five years the driver must follow a refresher course and pass an examination — the certificate will stipulate ‘national transport of UN 1202, 1203 and 1223 pursuant to Article 6(9) of Directive 94/55’.
RO-LT 1.4Subject:Transport of dangerous goods in tanks for elimination by incineration.
Reference to the Annex to the Directive:3.2.
Reference to the national legislation:Derogation 01 — 2002.
Content of the national legislation:By derogation from the table in chapter 3.2. it is permitted to use a tank-container with tank-code L4BH instead of tank-code L4DH for the carriage of UN 3130, water reactive liquid, toxic, III, n.o.s. under certain conditions.
Comments:This Regulation may only be used for the carriage of hazardous waste for a short distance.
RO-LT 1.5Subject:Carriage of waste to waste disposal plants.
Reference to the Annex of the Directive:5.2, 5.4, 6.1. (old Regulation: A5, 2X14, 2X12)
Content of the Annex of the Directive:Classification, marking and requirements concerning the packaging.
Reference to the national legislation:Arrêté royal relatif au transport de marchandises dangereuses par route.
Content of the national legislation:Instead of classifying wastes according to ADR, wastes are assigned to different groups (flammable solvents, paints, acids, batteries, etc.) to avoid dangerous reactions within one group. The requirements for construction of packagings are less restrictive.
Comments:this regulation may be used for the carriage of small quantities of waste to disposal plants.
RO-LT 1.6Subject:Adoption of RO-LT 14.5.
Reference to the national legislation:—
RO-LT 1.7Subject:Adoption of RO-LT 14.6.
Reference to the national legislation:—
RO-LT 1.8Subject:Adoption of RO-LT 15.2.
Reference to the national legislation:—
DENMARKRO-LT 2.1Subject:UN 1202, 1203, 1223 and class 2 — no transport document.
Reference to the Annex to the Directive:5.4.1.
Content of the Annex to the Directive:Transport document needed.
Reference to the national legislation:Bekendtgørelse nr. 729 af 15/08/2001 om vejtransport af farligt gods.
Content of the national legislation:When transporting mineral oil products in class 3, UN 1202, 1203 and 1223 and gases in class 2 in connection with distribution (goods to be delivered to two or more recipients and collection of returned goods in similar situations), transport document is not requisite provided the instructions in writing, besides the information requested in ADR, contain information about UN-No, name and class.
Comments:The reason for having a national derogation as above-mentioned is the development of electronic equipment making it possible for e.g. the oil companies using electronic equipment continuously to transmit information to the vehicles containing information about the customers. As this information is not available at the beginning of the transport and will be forwarded to the vehicle during the transport, it is not possible — before the transport begins — to draw up the transport documents. These kind of transports are restricted to limited areas.
Currently a derogation for Denmark for a similar provision under Article 6.10.
GERMANYRO-LT 3.1Subject:Waive of certain indications in the transport document (n2).
Reference to the Annex to the Directive:5.4.1.1.1.
Content of the Annex to the Directive:Contents of the transport document.
Reference to the national legislation:Gefahrgut-Ausnahmeverordnung – GGAV 2002 vom 6.11.2002 (BGBl. I S. 4350), geändert durch Artikel 2 der Verordnung vom 28.4.2003 (BGBl. I S. 595); Ausnahme 18.
Content of the national legislation:For all classes except classes 1 (except 1.4S), 5.2. and 7:
No indication needed in the transport document

(a) | for the consignee in case of local distribution (except for full load and for transport with certain routings);
(b) | for the amount and types of packagings, if 1.1.3.6. is not applied and if the vehicle is in conformity with all provisions of Annex A and B;
(c) | for empty uncleaned tanks the transport document of the last load is sufficient.Comments:Applying all provisions would not be practicable in concerned kind of traffic.
Derogation is registered by the European Commission as No 22. (under 6.10).
RO-LT 3.2Subject:Transportation of Class 9 PCB-contaminated materials in bulk.
Reference to the Annex to the Directive:7.3.1.
Content of the Annex to the Directive:Transportation in bulk.
Reference to the national legislation:Gefahrgut-Ausnahmeverordnung – GGAV 2002 vom 6.11.2002 (BGBl. I S. 4350), geändert durch Artikel 2 der Verordnung vom 28.4.2003 (BGBl. I S. 595); Ausnahme 11.
Content of the national legislation:Authorisation for transportation in bulk in vehicle swap bodies or containers sealed to be impermeable to fluids or dust.
Comments:Derogation 11 limited to 31 December 2004; as from 2005, same provisions in ADR and RID.
See also Multilateral Agreement M137.
List No 4*.
RO-LT 3.3Subject:Transportation of packaged hazardous waste.
Reference to the Annex of the Directive:Parts 1 to 5.
Content of the Annex of the Directive:Classification, packaging and marking.
Reference to the national legislation:Gefahrgut-Ausnahmeverordnung – GGAV 2002 vom 6.11.2002 (BGBl. I S. 4350), geändert durch Artikel 2 der Verordnung vom 28.4.2003 (BGBl. I S. 595); Ausnahme 20.
Content of the national legislation:Classes 2 to 6.1, 8 und 9: Combined packaging and transportation of hazardous waste in packs and IBCs; waste must be packaged in internal packagings (as collected) and categorised in specific waste groups (avoidance of dangerous reactions within a waste group); use of special written instructions relating to the waste groups and as a waybill; collection of domestic and laboratory waste, etc.
Comments:List No 6*.
GREECERO-LT 4.1Subject:Derogation on safety requirements for fixed tanks (tank-vehicles), registered before 31 December 2001, for the local transport or small quantities of some categories of dangerous goods.
Reference to the Annex of the Directive:1.6.3.6, 6.8.2.4.2, 6.8.2.4.3, 6.8.2.4.4, 6.8.2.4.5, 6.8.2.1.17-6.8.2.1.22, 6.8.2.1.28, 6.8.2.2, 6.8.2.2.1, 6.8.2.2.2.
Content of the Annex of the Directive:Requirements for the construction, equipment, type approval, inspections and tests, and marking of fixed tanks (tank-vehicles), demountable tanks and tank containers and tank swap bodies, with shells made of metallic materials, and battery-vehicles and multiple element gas containers (MEGCs).
Reference to the national legislation:Τεχνικές Προδιαγραφές κατασκευής, εξοπλισμού και ελέγχων των δεξαμενών μεταφοράς συγκεκριμένων κατηγοριών επικινδύνων εμπορευμάτων για σταθερές δεξαμενές (οχήματα-δεξαμενές), αποσυναρμολογούμενες δεξαμενές που βρίσκονται σε κυκλοφορία. (Requirements for the construction, equipment, inspections and tests of fixed tanks (tank-vehicles), demountable tanks being in circulation, for some categories of dangerous goods.)
Content of the national legislation:Transitional provision: Fixed tanks (tank-vehicles), demountable tanks and tank containers first registered in our country between 1 January 1985 and 31 December 2001 may still be in use until 31 December 2010. This transitional provision concerns vehicles for the transport of the following dangerous materials (UN: 1202, 1268, 1223, 1863, 2614, 1212, 1203, 1170, 1090, 1193, 1245, 1294, 1208, 1230, 3262, 3257). This transport is supposed for small quantities or as local transport for vehicles registered at the above referenced period. This transitional period will be in force for tank vehicles adapted according to:

1. | ADR paragraphs for inspection and tests, 6.8.2.4.2, 6.8.2.4.3, 6.8.2.4.4, 6.8.2.4.5, (ADR 1999: 211.151, 211.152, 211.153, 211.154).
2. | Minimum shell thickness 3 mm for tanks with shells compartment capacity up to 3 500 lt and at least 4 mm thickness of mild steel for tanks with compartments with capacity up to 6 000 litres, regardless the type or thickness of the partitions.
3. | If the used material is aluminium or other metal, tanks should fulfil the requirements for thickness and other technical specifications that derive from technical drawings approved from the local authority of the country where were previously registered. In case of absence of technical drawings, tanks should fulfil the requirements of paragraph 6.8.2.1.17. (211.127).
4. | Tanks should fulfil marginal-paragraphs 211.128, 6.8.2.1.28. (211.129), paragraph 6.8.2.2. with sub-paragraphs 6.8.2.2.1. and 6.8.2.2.2. (211.130, 211.131).More precisely, the tank-vehicles with mass less than 4 tonnes used for local transport of gas oil only (UN 1202), first registered before 31 December 2002, if their shell thickness is lower than 3 mm, they are permitted to be in use only if they are transformed according to the marginal 211.127. (5)b4 (6.8.2.1.20).
RO-LT 4.2Subject:Derogation on Base Vehicle construction requirements, regarding vehicles intended for the local transport of dangerous goods first registered before 31 December 2001.
Reference to the Annex to the Directive:ADR 2001: 9.2, 9.2.3.2, 9.2.3.3.
Content of the Annex to the Directive:Requirements concerning the construction of Base Vehicles.
Reference to the national legislation:Τεχνικές Προδιαγραφές ήδη κυκλοφορούντων οχημάτων που διενεργούν εθνικές μεταφορές ορισμένων κατηγοριών επικινδύνων εμπορευμάτων. (Technical requirements of vehicles already in use, intended for local transport of certain dangerous goods categories.)
Content of the national legislation:The Derogation applies to vehicles intended for the local transport of dangerous goods (categories UN 1202, 1268, 1223, 1863, 2614, 1212, 1203, 1170, 1090, 1193, 1245, 1294, 1208, 1230, 3262 and 3257), which were first registered before 31 December 2001.
The abovementioned vehicles shall comply with the requirements of Chapter 9 (paragraphs 9.2.1. to 9.2.6) of the Annex B of the Directive 94/55/EC with the following deviations.
Comply with requirements of paragraph 9.2.3.2. necessarily only in case the vehicle is equipped with an antilock braking system by vehicle manufacturer and shall be fitted with an endurance braking system as defined in 9.2.3.3.1. but not necessarily complying with paragraphs 9.2.3.3.2. and 9.2.3.3.3.
The electrical supply to the tachograph shall be provided via a safety barrier connected directly to the battery (marginal 220 514) and the electrical equipment of the mechanism for lifting a bogie axle shall be installed where it has first been installed by the vehicle manufacturer and must be protected in an appropriate sealed housing (marginal 220 517).
Specific, tank-vehicles with maximum mass less than 4 tonnes intended for local transport of diesel-heating oil (UN: 1202) shall comply with requirements of paragraphs 9.2.2.3, 9.2.2.6, 9.2.4.3. and 9.2.4.5. but not necessarily with the other ones.
Comments:The number of the abovementioned vehicles is small, when compared with the total number of already registered vehicles and in addition are intended for local transport only. The form of the derogation requested, the size of the vehicle fleet in question and the type of goods transported do not create a road safety problem.
SPAINRO-LT 5.1Subject:Special equipment for distribution of anhydrous ammonia.
Reference to the Annex to the Directive:6.8.2.2.2.
Content of the Annex to the Directive:In order to avoid any loss of contents in the event of damage to the external fittings (pipes, lateral shut-off devices), the internal stop valve and its seating must be protected against the danger of being wrenched off by external stresses or be so designed as to resist such stresses. The filling and discharge devices (including flanges or threaded plugs) and protective caps (if any) must be capable of being secured against any unintended opening.
Reference to the national legislation:Real Decreto 2115/1998. Anejo 1. Apartado 3.
Content of the national legislation:Tanks used for agricultural purposes for the distribution and application of anhydrous ammonia which were brought into service before 1 January 1992 may be equipped with external, instead of internal, safety fittings, provided they offer protection at least equivalent to the protection provided by the wall of the tank.
Comments:Before 1 January 1992 a type of tank equipped with external safety fittings was used exclusively in agriculture to apply anhydrous ammonia directly onto the land. Various tanks of this kind are still in use today. They are rarely driven, laden, on the road, but are used solely for fertiliser-spreading in large farms.
FRANCERO-LT 6.1Subject:Utilisation of maritime document as transport document for short-distance trips following unloading of vessel.
Reference to the Annex to the Directive:5.4.1.
Content of the Annex to the Directive:Information to appear in the document used as transport document for hazardous goods.
Reference to the national legislation:Arrêté du 1erjuin 2001 relatif au transport de marchandises dangereuses par route (Decree of 1 June 2001 on the transport of hazardous goods by road, ‘ADR-Decree’) – Article 23-4.
Content of the national legislation:The maritime document is used as transport document within a radius of 15 km.
RO-LT 6.2Subject:Transport of Class 1 articles together with hazardous materials in other classes (91).
Reference to the Annex to the Directive:7.5.2.1.
Content of the Annex to the Directive:Prohibition against loading parcels with different hazard labels together.
Reference to the national legislation:Arrêté du 1erjuin 2001 relatif au transport de marchandises dangereuses par route (Decree of 1 June 2001 on the transport of hazardous goods by road, ‘ADR-Decree’) – Article 26.
Content of the national legislation:Possibility of transporting simple or assembled detonators and goods not in Class 1 together, subject to certain conditions and for distances less than or equal to 200 km in France.
RO-LT 6.3Subject:Transport of fixed LPG storage tanks (18).
Reference to the Annex to the Directive:Annexes A and B.
Reference to the national legislation:Arrêté du 1erjuin 2001 relatif au transport de marchandises dangereuses par route (Decree of 1 June 2001 on the transport of hazardous goods by road, ‘ADR-Decree’) – Article 30.
Content of the national legislation:The transport of fixed LPG storage tanks is subject to specific rules. Applicable only to short distances.
RO-LT 6.4Subject:Specific conditions relating to driver training and the approval of vehicles used for agricultural transport (short distances).
Reference to the Annex to the Directive:6.8.3.2; 8.2.1. and 8.2.2.
Content of the Annex to the Directive:Tank equipment and driver training.
Reference to the national legislation:Arrêté du 1erjuin 2001 relatif au transport de marchandises dangereuses par route (Decree of 1 June 2001 on the transport of hazardous goods by road, ‘ADR-Decree’) – Article 29.2. – Annex D4.
Content of the national legislation:Specific provisions concerning the approval of vehicles. Special training for drivers.
IRELANDRO-LT 7.1Subject:Exemption from the requirement of 5.4.1.1.1, to have (i) the names and addresses of the consignees, (ii) the number and description of the packages, and (iii) the total quantity of dangerous goods in the transport document, where kerosene, diesel fuel or liquefied petroleum gas bearing the respective substance identification numbers UN 1223, UN1202 and UN 1965 are being carried to the end user.
Reference to the Annex to the Directive:5.4.
Content of the Annex to the Directive:Documentation.
Reference to the national legislation:Regulation 82(2) of the Carriage of Dangerous Goods by Road Regulations, 2004.
Content of the national legislation:Where kerosene, diesel fuel or liquefied petroleum gas, bearing the respective substance identification numbers UN 1223, UN 1202 and UN 1965 as specified in Appendix B.5. of Annex B to the ADR, are being carried to the end user, it is not necessary to include the name and address of the consignee, the number and description of the packages, Intermediate Bulk Containers or receptacles, or the total quantity being carried, on the transport unit.
Comments:In the case of delivery of home heating oil to domestic customers, it is a common practice to ‘top up’ the customer’s storage tank — hence the actual delivery is unknown and also the number of customers (in any one run) is also unknown at the time the loaded tanker begins its journey. In the case of delivery of cylinders of LPG to households, it is a common practice to replace empty cylinders with full ones — hence the number of customers and their individual consignments are unknown at the beginning of the transport operation.
RO-LT 7.2Subject:Exemption to allow the transport document, required in 5.4.1.1.1, to be that for the last load in the case of the transport of empty uncleaned tanks.
Reference to the Annex to the Directive:5.4.
Content of the Annex to the Directive:Documentation.
Reference to the national legislation:Regulation 82(3) of the Carriage of Dangerous Goods by Road Regulations, 2004.
Content of the national legislation:In the case of the carriage of empty uncleaned tanks, the Transport Document for the last load is sufficient.
Comments:Particularly in the case of delivery of petrol and/or diesel fuel to petrol stations, the road tanker returns directly to the oil depot (to be loaded up again for the next deliveries) immediately after delivery of the last load.
RO-LT 7.3Subject:Exemption to allow the loading and unloading of dangerous goods, to which the special provision CV1 in 7.5.11. or S1 in 8.5. is assigned, in a public place without special permission from the competent authorities.
Reference to the Annex to the Directive:7.5. and 8.5.
Content of the Annex to the Directive:Additional provisions concerning the loading, unloading and handling.
Reference to the national legislation:Regulation 82(5) of the Carriage of Dangerous Goods by Road Regulations, 2004.
Content of the national legislation:Loading and unloading of dangerous goods in a public place is permitted without special permission from the competent authority, in derogation from the requirements of 7.5.11. or 8.5.
Comments:For national transport within the State, this provision places a very onerous burden on the competent authorities.
RO-LT 7.4Subject:Exemption to permit the transport of Emulsion Explosive Matrix, with substance identification number UN 3375, in tanks.
Reference to the Annex to the Directive:4.3.
Content of the Annex to the Directive:Use of tanks, etc.
Reference to the national legislation:Regulation 82(6) of the Carriage of Dangerous Goods by Road Regulations, 2004.
Content of the national legislation:The carriage of Emulsion Explosive Matrix, bearing the substance identification number UN 3375, is permitted in tanks.
Comments:The matrix, although classified as a solid, is not in a powdery or granular form.
RO-LT 7.5Subject:Exemption from the ‘mixed loading prohibition’ of 7.5.2.1. for articles of Compatibility Group B and substances and articles of Compatibility D on same vehicle with dangerous goods, in tanks, of Classes 3, 5.1. and 8.
Reference to the Annex to the Directive:7.5
Content of the Annex to the Directive:Provisions concerning loading, unloading and handling.
Reference to the national legislation:Regulation 82(7) of the Carriage of Dangerous Goods by Road Regulations, 2004.
Content of the national legislation:Packages containing articles of Compatibility Group B of ADR Class 1 and packages containing substances and articles of Compatibility Group D of ADR Class 1 may be carried on the same vehicle with dangerous goods of ADR Classes 3, 5.1. or 8 provided — (a) the said packages of ADR Class 1 are carried in separate containers/compartments of a design approved, and under the conditions required, by the competent authority, and (b) the said substances of ADR Classes 3, 5.1. or 8 are carried in vessels meeting the requirements of the competent authority as regards their design, construction, testing, examination, operation and use.
Comments:To permit, under conditions approved by the competent authority, the loading of articles and substances of Class 1 Compatibility Groups B and D on the same vehicle with dangerous goods, in tanks, of Classes 3, 5.1. and 8 — i.e. Pump Trucks.
RO-LT 7.6Subject:Exemption from requirement in 4.3.4.2.2, which requires flexible filling and discharge pipes which are not permanently connected to the shell of a tank-vehicle to be empty during transport.
Reference to the Annex to the Directive:4.3.
Content of the Annex to the Directive:Use of tank-vehicles.
Reference to the national legislation:Regulation 82(8) of the Carriage of Dangerous Goods by Road Regulations, 2004.
Content of the national legislation:Flexible hose reels (including fixed pipelines associated with them) attached to tank-vehicles engaged in the retail distribution of petroleum products with substance identification numbers UN 1202, UN 1223, UN 1011 and UN 1978 are not required to be empty during carriage by road provided adequate measures are taken to prevent any loss of contents.
Comments:Flexible hoses fitted to home delivery tank-vehicles must remain full at all times even during transport. The discharge system is known as a ‘wet-line’ system that requires the tank-vehicle’s meter and hose to be primed so as to ensure the customer receives the correct quantity of product.
RO-LT 7.7Subject:Exemption from some requirements of Chapters 5.4.0, 5.4.1.1.1. and 7.5.11. of the ADR for the transport in bulk of Ammonium Nitrate Fertiliser UN 2067 from ports to consignees.
Reference to the Annex to the Directive:5.4.0, 5.4.1.1.1. and 7.5.11.
Content of the Annex to the Directive:The requirement for a separate transport document, with the correct total quantity for the particular load included, for each transport journey; and the requirement for the vehicle to be cleaned before and after the journey.
Reference to the national legislation:Proposed amendment to ‘Carriage of Dangerous Goods by Road Regulations, 2004’.
Content of the national legislation:Proposed derogation to allow modifications to ADR requirements on the transport document and vehicle cleaning; to take account of the practicalities of bulk transport from port to consignee.
Comments:The ADR provisions require (a) a separate transport document, containing the total mass of dangerous goods carried for the particular load, and (b) the Special Provision ‘CV24’ on cleaning for each and every load being transported between the port and the consignee during the unloading of a bulk ship. As the transport is local and as it concerns the unloading of a bulk ship, involving multiple transport loads [on the same or consecutive days] of the same substance between the bulk ship and the consignee; a single transport document, with an approximate total mass of each load, should suffice and it should not be necessary to require the Special Provision ‘CV24’.
THE NETHERLANDSRO-LT 10.1Subject:Scheme for the transport of domestic hazardous waste 2002.
Reference to the Annex to the Directive:1.1.3.6; 3.3; 4.1.4; 4.1.6; 4.1.8; 4.1.10; 5.2.2; 5.4.0; 5.4.1; 5.4.3; 7.5.4; 7.5.7; 8.1.2.1, subsections a) and b); 8.1.5, subsection c); 8.3.6.
Content of the Annex to the Directive:
1.1.3.6: Exemptions in connection with the transported quantities per transport unit.
3.3: Special provisions applicable to specified substances or objects.
4.1.4: List with packing instructions;4.1.6: Special packaging requirements for class 2 goods;4.1.8: Special packaging requirements for infectious substances;4.1.10: Special requirements for collective packaging.
5.2.2: Labelling of transport packages;5.4.0: Any goods transported under the ADR scheme must be accompanied by the documentation prescribed in this chapter, where applicable, unless an exemption has been granted under points 1.1.3.1. to 1.1.3.5;5.4.1: Transit document for dangerous goods along with related information;5.4.3: written instructions.
7.5.4: Precautions with regard to food, other articles of consumption and animal feedingstuffs;7.5.7: Handling and stowage.
8.1.2.1: In addition to the documentation required by law, the following documents must be carried on board the transport unit:a. the transit documents referred to in 5.4.1. and covering all the dangerous goods transported and, where applicable, the container loading certificate as stipulated in point 5.4.2;b. the written instructions as set out in point 5.4.3, relating to all the dangerous goods transported;8.1.5: Each transport unit carrying dangerous goods must be fitted with:c.the equipment needed to permit the carrying-out of the supplementary and special measures as indicated in the written instructions referred to in point 5.4.3.8.3.6: Leaving the engine running during loading and unloading.
Reference to the national legislation:Artikel 3 van de Regeling vervoer huishoudelijk gevaarlijk afval 2002.
Content of the national legislation:Article 3
The following sections of the ADR shall not apply:

a. | 1.1.3.6;
b. | 3.3;
c. | 4.1.4; 4.1.6; 4.1.8; 4.1.10;
d. | 5.2.2; 5.4.0; 5.4.1; 5.4.3;
e. | 7.5.4; 7.5.7;
f. | 8.1.2.1. subsections a) and b); 8.1.5. subsection c); 8.3.6.Comments:The scheme has been designed in such a way as to enable private citizens to present ‘small chemical waste’ at a single location. This applies to residual substances such as dye waste, for instance. The danger level is minimised by the choice of means of transport, involving,inter alia, the use of special transport elements and ‘no smoking’ notices clearly visible to members of the public.
In view of the limited quantities offered and the specialised nature of the packaging, this article excludes a number of sections of the ADR. Supplementary rules are laid down elsewhere in the scheme.
RO-LT 10.2Subject:Scheme for transport of domestic hazardous waste 2002.
Reference to the Annex to the Directive:1.1.3.6.
Content of the Annex to the Directive:Exemptions in connection with the transported quantities per transport unit.
Reference to the national legislation:Artikel 10, onderdeel a, en 16, onderdeel b, van de Regeling vervoer huishoudelijk gevaarlijk afval 2002.
Content of the national legislation:

| 10a. | The attendant’s certificate of professional competence and the note referred to in Article 16(1)(b) are both on board the vehicle;
| 16b. | The vehicle attendant holds the qualification ‘transport of hazardous waste’ issued by the CCV (Drivers’ Certification Board).Comments:Because of the wide range of domestic hazardous waste involved, the transport operator must have a certificate of professional competence, notwithstanding the small quantities of waste presented. An additional requirement is that the transport operator has been issued with a qualification for the transport of hazardous waste.
One of the reasons for this is to ensure that the transport operator does not, for instance, pack acids and bases together and that he knows how to respond properly to incidents.
RO-LT 10.3Subject:Scheme for the transport of domestic hazardous waste 2002.
Reference to the Annex to the Directive:1.1.3.6.
Content of the Annex to the Directive:Exemptions in connection with the transported quantities per transport unit.
Reference to the national legislation:Artikel 10b van de Regeling vervoer huishoudelijk gevaarlijk afval 2002.
Content of the national legislation:Article 10 b
The following are present on board the vehicle: b. written instructions and information compiled in accordance with the annex to the act setting up the scheme.
Comments:As the scheme excludes exemption from section 1.1.3.6. of the ADR scheme, written instructions must also accompany small quantities. This is deemed necessary because of the wide range of hazardous waste presented and the fact that those presenting the waste (private citizens) are unfamiliar with the danger level involved.
RO-LT 10.4Subject:Scheme for the transport of domestic hazardous waste 2002.
Reference to the Annex to the Directive:6.1
Content of the Annex to the Directive:Provisions on the construction and testing of packaging.
Reference to the national legislation:Artikel 6 van de Regeling vervoer huishoudelijk gevaarlijke afval 2002.
Content of the national legislation:Article 6

1. | The domestic hazardous waste is to be presented only in a hermetically sealed packaging that is appropriate for the substance in question, and:(a)for objects coming under category 6.2: a packaging guaranteed not to cause injury upon presentation;(b)for domestic hazardous waste of industrial origin: a box having a capacity of not more than 60 litres, in which the waste substances are separated according to danger category (kga-box). | (a) | for objects coming under category 6.2: a packaging guaranteed not to cause injury upon presentation; | (b) | for domestic hazardous waste of industrial origin: a box having a capacity of not more than 60 litres, in which the waste substances are separated according to danger category (kga-box).
(a) | for objects coming under category 6.2: a packaging guaranteed not to cause injury upon presentation;
(b) | for domestic hazardous waste of industrial origin: a box having a capacity of not more than 60 litres, in which the waste substances are separated according to danger category (kga-box).
2. | The packaging is free, on the outside, from domestic hazardous waste.
3. | The name of the substance is indicated on the packaging.
4. | For each collection, only one box within the meaning of point 1, subsection b, will be accepted.Comments:This article results from Article 3 in which particular sections of the ADR are declared non-applicable. Under this scheme, there is no need for approved packaging as provided for in section 6.1. of the ADR. This is because of the limited quantities of dangerous substances involved. Instead, a number of rules are laid down in the article including a requirement to the effect that the hazardous substances be delivered in sealed containers so as to prevent seepage from the packaging.
RO-LT 10.5Subject:Scheme for the transport of domestic hazardous waste 2002.
Reference to the Annex to the Directive:6.1
Content of the Annex to the Directive:Provisions on the construction and testing of packaging.
Reference to the national legislation:Artikel 7, tweede lid, van de Regeling vervoer huishoudelijk gevaarlijk afval 2002.
Content of the national legislation:Article 7.2
The vehicle has a load compartment that is separated from the driver’s compartment by a solid thick wall or, alternatively, a load compartment that is not an integral part of the vehicle.
Comments:Under this scheme, it is not necessary to have an approved packaging as stipulated in section 6.1. of the ADR. This is because of the limited quantities of dangerous substances involved. Accordingly, this Article contains an additional requirement designed to prevent toxic fumes from leaking into the driver’s compartment.
RO-LT 10.6Subject:Scheme for the transport of domestic hazardous waste 2002.
Reference to the Annex to the Directive:6.1
Content of the Annex to the Directive:Provisions on the construction and testing of packaging.
Reference to the national legislation:Artikel 8, eerste lid, van de Regeling vervoer huishoudelijk gevaarlijk afval 2002.
Content of the national legislation:Article 8.1
The load compartment of a closed vehicle has an air extractor, which is kept permanently on, at the top and is fitted with apertures underneath.
Comments:Under this scheme, it is not necessary to have an approved packaging as stipulated in section 6.1. of the ADR. This is because of the limited quantities of dangerous substances involved. Accordingly, this article contains an additional requirement designed to prevent the accumulation of toxic fumes in the load compartment.
RO-LT 10.7Subject:Scheme for the transport of domestic hazardous waste 2002.
Reference to the Annex to the Directive:6.1.
Content of the Annex to the Directive:Provisions on the construction and testing of packaging.
Reference to the national legislation:Artikel 9, eerste, tweede en derde lid, van de Regeling vervoer huishoudelijk gevaarlijk afval 2002.
Content of the national legislation:Article 9

1. | The vehicle is fitted with units which, during transport:(a)are protected against accidental displacement; and(b)are sealed with a lid and protected against accidental opening. | (a) | are protected against accidental displacement; and | (b) | are sealed with a lid and protected against accidental opening.
(a) | are protected against accidental displacement; and
(b) | are sealed with a lid and protected against accidental opening.
2. | Point 1, subsection b, is not applicable during transit for collection purposes or when the vehicle is stationary on its collection rounds.
3. | A sufficiently large clearance zone should be set aside in the vehicle so as to enable the domestic hazardous waste to be sorted and deposited in the different units.Comments:Under this scheme, it is not necessary to have an approved packaging as stipulated in section 6.1. of the ADR. This is because of the limited quantities of dangerous substances involved. This article seeks to provide a single guarantee through the use of units for storing the packagings, thereby ensuring an appropriate method of storage for each category of dangerous goods.
RO-LT 10.8Subject:Scheme for transport of domestic hazardous waste 2002.
Reference to the Annex to the Directive:6.1
Content of the Annex to the Directive:Provisions on the construction and testing of packaging.
Reference to the national legislation:Artikel 14 van de Regeling vervoer huishoudelijk gevaarlijke afval 2002.
Content of the national legislation:Article 14

1. | Domestic hazardous waste is exclusively transported in elements.
2. | There is a separate element for substances and objects in each class.
3. | With regard to class 8 substances and objects, there are separate elements for acids, bases and batteries.
4. | Spray cans may be placed in closable cardboard boxes provided that these boxes are transported in accordance with Article 9(1).
5. | If class 2 fire extinguishers have been collected, they may be placed in the same element as spray cans not packed in cardboard boxes.
6. | By derogation from Article 9(1), no lid is required for the transport of batteries, provided that they are placed in the element in such a way that all of the batteries’ openings are closed off and face upward.Comments:This article results from Article 3 in which particular sections of the ADR are declared non-applicable. Under this scheme, there is no need for approved packaging as provided for in section 6.1. of the ADR. This article lays down requirements for the elements in which domestic hazardous waste is temporarily stored.
RO-LT 10.9Subject:Scheme for transport of domestic hazardous waste 2002.
Reference to the Annex to the Directive:6.1.
Content of the Annex to the Directive:Provisions on the construction and testing of packaging.
Reference to the national legislation:Artikel 15 van de Regeling vervoer huishoudelijk gevaarlijke afval 2002.
Content of the national legislation:Article 15

1. | The elements, or boxes destined for transport of spray cans, should be clearly marked as follows:(a)for class 2 sprays collected in cardboard boxes: the word ‘SPUITBUSSEN’ [spray cans];(b)for class 2 fire extinguishers and spray cans: label No 2.2;(c)for class 3 fire extinguishers and spray cans: label No 3;(d)for class 4.1. paint waste: label No 4.1;(e)for class 6.1. noxious substances: label No 6.1;(f)for class 6.2. objects: label No 6.2;(g)for class 8 caustic substances and objects: label No 8; and furthermore:(h)for alkaline substances: the word ‘BASEN’ [bases];(i)for acidic substances: the word ‘ZUREN’ [acids];(j)for batteries: the word ‘ACCU’S’ [batteries]. | (a) | for class 2 sprays collected in cardboard boxes: the word ‘SPUITBUSSEN’ [spray cans]; | (b) | for class 2 fire extinguishers and spray cans: label No 2.2; | (c) | for class 3 fire extinguishers and spray cans: label No 3; | (d) | for class 4.1. paint waste: label No 4.1; | (e) | for class 6.1. noxious substances: label No 6.1; | (f) | for class 6.2. objects: label No 6.2; | (g) | for class 8 caustic substances and objects: label No 8; and furthermore: | (h) | for alkaline substances: the word ‘BASEN’ [bases]; | (i) | for acidic substances: the word ‘ZUREN’ [acids]; | (j) | for batteries: the word ‘ACCU’S’ [batteries].
(a) | for class 2 sprays collected in cardboard boxes: the word ‘SPUITBUSSEN’ [spray cans];
(b) | for class 2 fire extinguishers and spray cans: label No 2.2;
(c) | for class 3 fire extinguishers and spray cans: label No 3;
(d) | for class 4.1. paint waste: label No 4.1;
(e) | for class 6.1. noxious substances: label No 6.1;
(f) | for class 6.2. objects: label No 6.2;
(g) | for class 8 caustic substances and objects: label No 8; and furthermore:
(h) | for alkaline substances: the word ‘BASEN’ [bases];
(i) | for acidic substances: the word ‘ZUREN’ [acids];
(j) | for batteries: the word ‘ACCU’S’ [batteries].
2. | The same labels and texts are visibly displayed on the closable spaces within the vehicle where the elements may be placed.Comments:This article results from Article 3 in which particular sections of the ADR are declared non-applicable. Under this scheme, there is no need for approved packaging as provided for in section 6.1. of the ADR. This article lays down requirements for the identification of elements in which domestic hazardous waste is temporarily stored.
RO-LT 10.10Subject:Scheme for transport of domestic hazardous waste 2002.
Reference to the Annex to the Directive:7.5.4.
Content of the Annex to the Directive:Precautions with regard to food, other articles of consumption and animal feedingstuffs.
Reference to the national legislation:Artikel 13 van de Regeling vervoer huishoudelijk gevaarlijk afval 2002.
Content of the national legislation:Article 13

1. | The transport of food for humans and animal feedingstuffs at the same time as domestic hazardous waste is prohibited.
2. | The vehicle must be stationary during collection.
3. | An amber flashing light must be operated on the vehicle while it is moving or stationary for collection.
4. | During collection at a fixed location, indicated for this purpose, the engine must be switched off and, by derogation from point 3, the flashing light may be switched off.Comments:The prohibition in section 7.5.4. of the ADR is extended here because, given the wide range of substances presented, there is virtually always a class 6.1. substance present.
RO-LT 10.11Subject:Scheme for the transport of domestic hazardous waste 2002.
Reference to the Annex to the Directive:7.5.9.
Content of the Annex to the Directive:Ban on smoking.
Reference to the national legislation:Artikel 9, vierde lid, van de Regeling vervoer huishoudelijk gevaarlijk afval 2002.
Content of the national legislation:Article 9

| 4. | ‘No smoking’ notices must be clearly displayed on the sides and at the rear of the vehicle.Comments:Because the scheme covers the presentation of dangerous substances by private citizens, Article 9.4. stipulates that a ‘no smoking’ notice must be clearly displayed.
RO-LT 10.12Subject:Scheme for transport of domestic hazardous waste 2002.
Reference to the Annex to the Directive:8.1.5.
Content of the Annex to the Directive:Equipment of various types.
Every transport unit carrying hazardous goods must be fitted with:

(a) | at least one stop block for each vehicle with a size appropriate for the vehicle’s weight and the diameter of the wheels;
(b) | the equipment necessary to carry out the general measures indicated in the safety instructions referred to in 5.4.3, in particular:—two separate upright warning signals (e.g. reflective cones, emergency warning triangles, or flashing amber lights that are independent of the vehicle’s electrical installation);—a good quality safety jacket or safety clothing (e.g. as described in European standard EN 471) for every crew member;—a hand-held torch (see also 8.3.4) for every crew member;—protective breathing equipment in accordance with additional requirement S7 (see chapter 8.5) if this additional provision is applicable in accordance with the indication in column 19 of table A of chapter 3.2; | — | two separate upright warning signals (e.g. reflective cones, emergency warning triangles, or flashing amber lights that are independent of the vehicle’s electrical installation); | — | a good quality safety jacket or safety clothing (e.g. as described in European standard EN 471) for every crew member; | — | a hand-held torch (see also 8.3.4) for every crew member; | — | protective breathing equipment in accordance with additional requirement S7 (see chapter 8.5) if this additional provision is applicable in accordance with the indication in column 19 of table A of chapter 3.2;
— | two separate upright warning signals (e.g. reflective cones, emergency warning triangles, or flashing amber lights that are independent of the vehicle’s electrical installation);
— | a good quality safety jacket or safety clothing (e.g. as described in European standard EN 471) for every crew member;
— | a hand-held torch (see also 8.3.4) for every crew member;
— | protective breathing equipment in accordance with additional requirement S7 (see chapter 8.5) if this additional provision is applicable in accordance with the indication in column 19 of table A of chapter 3.2;
(c) | the equipment necessary to carry out the additional and special measures as indicated in the written instructions referred to in 5.4.3.Reference to the national legislation:Artikel 11 van de Regeling vervoer huishoudelijk gevaarlijk afval 2002.
Content of the national legislation:Article 11
A safety kit is carried on board within reach for each member of crew, comprising the following:

(a) | fully sealing safety goggles;
(b) | protective breathing mask;
(c) | acid-resistant, acid-proof overalls or apron;
(d) | synthetic-rubber gloves;
(e) | acid-proof, acid-resistant boots or safety shoes; and
(f) | an eye rinse bottle with distilled water.Comments:Because of the wide range of hazardous substances presented, extra requirements are imposed on mandatory safety equipment over and above those of section 8.1.5. of the ADR.
FINLANDRO-LT 13.1Subject:Modification of information in the transport document for explosive substances.
Reference to the Annex to the Directive:5.4.1.2.1(a).
Content of the Annex to the Directive:Special provisions for Class 1.
Reference to the national legislation:Liikenne- ja viestintäministeriön asetus vaarallisten aineiden kuljetuksesta tiellä (277/2002; 313/2003).
Content of the national legislation:In the transport document, it is allowed to use the number of detonators ((1 000 detonators correspond to 1 kg explosives) instead of actual net mass of explosive substances.
Comments:The information is considered sufficient for national transport. This derogation is used mainly for the blasting industry in small amounts in local transport.
Derogation is registered by the European Commission as number 31.
RO-LT 13.2Subject:Adoption of RO-LT 14.2.
Reference to the national legislation:To be specified in forthcoming Regulations.
RO-LT 13.3Subject:Adoption of RO-LT 14.7.
Reference to the national legislation:To be specified in forthcoming Regulations.
SWEDENRO-LT 14.1Subject:Carriage of hazardous waste to hazardous waste disposal plants.
Reference to the Annex to the Directive:2, 5.2. and 6.1.
Content of the Annex to the Directive:Classification, marking and labelling, and requirements for the construction and testing of packaging.
Reference to national legislation:Särskilda bestämmelser om vissa inrikes transporter av farligt gods på väg och i terräng.
Content of the national legislation:The legislation consists of simplified classification criteria, less restrictive requirements for the construction and testing of packaging, and modified labelling and marking requirements.
Instead of classifying hazardous waste according to ADR it is assigned to different waste groups. Each waste group contains substances that can, in accordance with ADR, be packed together (mixed packing).
Each package must be marked with the relevant waste group code instead of the UN number.
Comments:These regulations may only be used for the carriage of hazardous waste from public recycling sites to hazardous waste disposal plants.
RO-LT 14.2Subject:The name and address of the consignor in the transport document.
Reference to the Annex to the Directive:5.4.1.1.
Content of the Annex to the Directive:General information required in the transport document.
Reference to the national legislation:Särskilda bestämmelser om vissa inrikes transporter av farligt gods på väg och i terräng.
Content of the national legislation:National legislation states that the name and address of the consignor is not required if empty, uncleaned packaging is returned as a part of a distribution system.
Comments:Empty uncleaned packaging being returned will in most cases still contain small quantities of dangerous goods.
This derogation is mainly used by industries when returning empty uncleaned gas receptacles in exchange for full ones.
RO-LT 14.3Subject:Transport of dangerous goods in the close proximity of industrial site(s), including transport on public roads between various parts of the site(s).
Reference to the Annex to the Directive:Annexes A and B.
Content of the Annex to the Directive:Requirements for the transport of dangerous goods on public roads.
Reference to the national legislation:Särskilda bestämmelser om vissa inrikes transporter av farligt gods på väg och i terräng.
Content of the national legislation:Transport in the close proximity of industrial site(s), including transport on public roads between various parts of the site(s). The derogations concern the labelling and marking of packages, transport documents, drivers certificate and certificate of approval according to part 9.
Comments:There are several situations in which dangerous goods are transferred between premises situated on opposite sides of a public road. This form of transport does not constitute carriage of dangerous goods on a private road and should therefore be associated with the relevant requirements.
Compare also with the Directive 96/49/EC, Article 6(14).
RO-LT 14.4Subject:Transport of dangerous goods that have been seized by the authorities.
Reference to the Annex to the Directive:Annex A and B.
Content of the Annex to the Directive:Requirements for the transport of dangerous goods by road.
Reference to national legislation:Särskilda bestämmelser om vissa inrikes transporter av farligt gods på väg och i terräng.
Content of national legislation:Deviations from the regulations may be permitted if they are motivated by reasons of labour protection, unloading risks, submission of evidence, etc.
Deviations from the regulations are only permitted if satisfactory safety levels are met during normal conditions of carriage.
Comments:These derogations may only be applied by authorities seizing dangerous goods.
This derogation is intended for local transport. It could be transport of goods that have been seized by the police e.g. explosives or stolen property. The problem with these types of goods is that you can never be sure of classifications. In addition the goods are often not packed, marked or labelled in accordance with ADR. There are several hundred such transportations carried out by the police every year.
In the case of smuggled liquor, this must be transported from the place where it is seized to an evidence storage facility and then on to a facility for destruction, the latter two may be quite far apart from each other. The deviations permitted are: (a) each package does not need to be labelled, and (b) approved packages do not need to be used. However each pallet containing such packages must be correctly labelled. All other requirements must be fulfilled. There are approximately 20 such transportations each year.
RO-LT 14.5Subject:Transport of dangerous goods in and in close proximity to ports.
Reference to the Annex to the Directive:8.1.2, 8.1.5, 9.1.2.
Content of the Annex to the Directive:Documents to be carried on the transport unit; every transport unit carrying dangerous goods must be equipped with the specified equipment; vehicles approval.
Reference to the national legislation:Särskilda bestämmelser om vissa inrikes transporter av farligt gods på väg och i terräng.
Content of the national legislation:Documents (except for the driver’s certificate) need not to carried on the transport unit.
A transport unit need not be equipped with the equipment specified in 8.1.5.
Tractors need not certificate of approval.
Comments:Compare Directive 96/49/EC, Article 6(14).
RO-LT 14.6Subject:Inspectors’ ADR training certificate.
Reference to the Annex to the Directive:8.2.1
Content of the Annex to the Directive:Drivers of vehicles must receive training courses.
Reference to the national legislation:Särskilda bestämmelser om vissa inrikes transporter av farligt gods på väg och i terräng.
Content of the national legislation:Inspectors that perform the yearly technical inspection of the vehicle do not need to attend the training courses mentioned in 8.2. or hold the ADR training certificate.
Comments:In some cases vehicles being tested in the technical inspection may be carrying dangerous goods as load, e.g. uncleaned, empty tanks.
The requirements in 1.3. and 8.2.3. are still applicable.
RO-LT 14.7Subject:Local distribution of UN 1202, 1203 and 1223 in tankers.
Reference to the Annex to the Directive:5.4.1.1.6, 5.4.1.4.1
Content of the Annex to the Directive:For empty uncleaned tanks and tank-containers the description shall be according to 5.4.1.1.6.
The name and address of multiple consignees may be entered in other documents.
Reference to the national legislation:Särskilda bestämmelser om vissa inrikes transporter av farligt gods på väg och i terräng.
Content of the national legislation:For empty, uncleaned tanks or tank-containers the description in the transport document according to 5.4.1.1.6. is not needed if the amount of the substance in the loading plan is marked with 0.
The name and address of the consignees is not required in any document on board the vehicle.
RO-LT 14.8Subject:Transport of empty uncleaned storage tanks not intended as transport equipment.
Reference to the Annex to the Directive:5.4.1.1.1, 6.8, 8.2.2.8.1.
Content of the Annex to the Directive:Transport document, requirements for the construction, testing etc. for tanks, and drivers certificate.
Reference to the national legislation:Särskilda bestämmelser om vissa inrikes transporter av farligt gods på väg och i terräng.
Content of the national legislation:Substances of UN 1202, 1203, 1223 and 1965 can be transported in storage tanks not intended as transport equipment. The tanks must be emptied.
The transport unit must be marked like a tanker vehicle with the relevant substance. The driver must have a certificate in accordance with 8.2.2.7.1.
Comments:This derogation is applied when storage tanks must be moved for instance for repair or maintenance purposes.
The reason for this derogation is to avoid the risk and environmental impact associated with the cleaning of empty tanks prior to transport.
This derogation applies to small quantities. Often this type of transport is local, but in rare cases such transport can be over 300 km in low-populated Northern Sweden.
Transport conditions: Equipment mounted on the storage tank must not be placed so that it is susceptible to damage during transport. Documents showing that the storage tank is approved for the relevant substance must accompany the vehicle. The bindings and fastenings used to secure the storage tank to the vehicle must be able to hold a tank weighing twice that of the storage tank being transported. Flammables cannot be carried as load on the same vehicle as the tank.
RO-LT 14.9Subject:Local transport in relation to agriculture sites or construction sites.
Reference to the Annex to the Directive:5.4, 6.8. and 9.1.2.
Content of the Annex to the Directive:Transport document; Construction of tanks; Certificate of approval.
Reference to the national legislation:Särskilda bestämmelser om vissa inrikes transporter av farligt gods på väg och i terräng.
Content of the national legislation:Local transport in relation to agriculture sites or construction sites need not fulfil some regulations:

— | the dangerous goods declaration is not required,
— | older tanks/containers not constructed according to chapter 6.8. but according to older national legislation and fitted on crew wagons may still be used,
— | older tankers, not fulfilling the requirements in 6.7. or 6.8, intended for the transport of substances of UN 1268, 1999, 3256 and 3257, with or without road surface coating equipment, may still be used for local transport and in close proximity to road work places,
— | certificate of approval for crew wagons and tankers with or without road surface coating equipment are not required.Comments:A crew wagon is a kind of caravan for a work crew with a crew room and fitted with a non approved tank/container for diesel fuel intended for the operation of forestry tractors.
RO-LT 14.10Subject:Tank transport of explosives.
Reference to the Annex to the Directive:4.1.4.
Content of the Annex to the Directive:Explosives may only be packed in packagings in accordance with 4.1.4.
Reference to the national legislation:Appendix S – Specific regulations for the domestic transport of dangerous goods by road issued in accordance with the Transport of Dangerous Goods Act and the Swedish regulation SÄIFS 1993: 4.
Content of the national legislation:The national competent authority will approve vehicles intended for tank transport of explosives. Tank transport is permissible only for those explosives listed in the regulation or by special authorisation from the competent authority.
A vehicle loaded with explosives in tanks must be marked and labelled in accordance with 5.3.2.1.1, 5.3.1.1.2. and 5.3.1.4. Only one vehicle in the transport unit may contain dangerous goods.
Comments:This is only applicable for domestic transport and the transport is mostly of a local nature.
The regulations in question were in force before Sweden joined the European Union.
Only two companies perform transport with expolosives in tank-vehicles. In the near future transition into emulsions is expected.
Old derogation No 84.
RO-LT 14.11Subject:Driver’s licence
Reference to the Annex to the Directive:8.2.
Content of the Annex to the Directive:Requirements concerning the training of the vehicle crew.
Reference to the national legislation:Appendix S – Specific regulations for the domestic transport of dangerous goods by road issued in accordance with the Transport of Dangerous Goods Act.
Content of the national legislation:Driver training is not permitted with any vehicle referred to in 8.2.1.1.
Comments:Local transport.
THE UNITED KINGDOMRO-LT 15.1Subject:Crossing of public roads by vehicles carrying dangerous goods (N8).
Reference to the Annex to the Directive:Annexes A and B.
Content of the Annex to the Directive:Requirements for the carriage of dangerous goods on public roads.
Reference to the national legislation:Carriage of Dangerous Goods by Road Regulations 1996, Regulation 3 Schedule 2 (3)(b); Carriage of Explosives by Road Regulations 1996, Regulation 3(3)(b).
Content of the national legislation:Disapplication of the dangerous goods regulations to carriage within private premises separated by a road.
Comments:Such a situation can easily occur where goods are transferred between private premises situated on both sides of a road. They do not constitute carriage of dangerous goods on a public road in the normal sense of the term, and none of the provisions of the dangerous goods regulations should apply in such a case.
RO-LT 15.2Subject:Exemption from prohibition of driver or driver’s assistant opening packages of dangerous goods in a local distribution chain from a local distribution depot to a retailer or end user and from the retailer to the end user (except for Class 7) (N11).
Reference to the Annex to the Directive:8.3.3.
Content of the Annex to the Directive:Prohibition of driver or driver’s assistant opening packages of dangerous goods.
Reference to the national legislation:Carriage of Dangerous Goods by Road Regulations 1996, Regulation 12 (3).
Content of the national legislation:Prohibition of opening packages is qualified by the proviso ‘Unless authorised to do so by the operator of the vehicle’.
Comments:If taken literally, the prohibition in the Annex as worded can create serious problems for retail distribution.

Pending: 32004D0558

23.7.2004 EN Official Journal of the European Union L 249/20
(1) Infectious bovine rhinotracheitis is the description of the most prominent clinical signs of the infection with the bovine herpesvirus type 1 (BHV1). As many infections with that virus run a subclinical course, control measures should be directed to the eradication of the infection rather than to the suppression of symptoms.
(2) Annex E (II) to Directive 64/432/EEC lists ‘infectious bovine rhinotracheitis’ among the diseases for which national control programmes may be approved and additional guarantees requested.
(3) Germany had submitted a programme conducted with the aim of eradicating the BHV1 infection in all parts of its territory, which complies with the criteria set out in Article 9(1) of Directive 64/432/EEC and provides for rules for the national movement of bovine animals which are equivalent to those previously implemented in Austria, the Province of Bolzano in Italy and Sweden which were successful in eradicating the disease from those countries.
(4) The programme presented by Germany and, as requested by that Member State, the additional guarantees in relation to trade in bovine animals in order to secure the success of that programme were approved by Decision 2004/215/EC of 1 March 2004 implementing Council Directive 64/432/EEC as regards additional guarantees for intra-Community trade in bovine animals relating to infectious bovine rhinotracheitis and the approval of the eradication programmes presented by certain Member States(2).
(5) Additional guarantees exist as regards Denmark, Austria, Finland and Sweden as well as Italy, concerning the province of Bolzano. Those Member States consider that their territory is free from infectious bovine rhinotracheitis and Italy takes the same view for the Province of Bolzano. In accordance with Article 10(1) of Directive 64/432/EEC, they submitted supporting documentation to the Commission, in particular substantiating that monitoring of the situation is continued.
(6) To Member States or regions thereof that are recognised as being free of that disease and which are currently listed in the Annex to Commission Decision 93/42/EEC(3)only minimum requirements for the dispatch of bovine animals for breeding and production to other Member States should apply.
(7) For the standardisation of BHV1 tests in laboratories the World Organisation for Animal Health (OIE) has adopted a strong positive, a weak positive and negative serum as OIE international standards for BHV1 tests which are available at the OIE Reference Laboratories for infectious bovine rhinotracheitis mentioned in the Manual of Standards for Diagnostic Tests and Vaccines(4).
(8) Problems have been encountered in relation to intra-Community trade in bovine animals originating in Member States of different status with regard to infectious bovine rhinotracheitis.
(9) For reasons of clarity and in order to ensure the linguistic consistency of the measures, it is appropriate to combine in a single Decision the approval of the German programme and the additional guarantees for infectious bovine rhinotracheitis and to repeal Decision 2004/215/EC.
(10) The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health,
(a) they must come from a holding on which, according to official information, no clinical or pathological evidence of infectious bovine rhinotracheitis has been recorded for the past 12 months;
(b) they must have been isolated in a facility approved by the competent authority for 30 days immediately prior to movement and all bovine animals in the same isolation facility must have remained free of clinical signs of infectious bovine rhinotracheitis during that period;
(c) they and all other bovine animals in the same isolation facility must have been subjected with negative results to a serological test carried out on blood samples, taken not earlier than 21 days after their arrival at the isolation facility, for the detection of the following antibodies:(i)in the case of vaccinated bovine animals, antibodies against the gE-glycoprotein of the BHV1; or(ii)in the case of unvaccinated bovine animals, antibodies against the entire BHV1. (i) in the case of vaccinated bovine animals, antibodies against the gE-glycoprotein of the BHV1; or (ii) in the case of unvaccinated bovine animals, antibodies against the entire BHV1.
(i) in the case of vaccinated bovine animals, antibodies against the gE-glycoprotein of the BHV1; or
(ii) in the case of unvaccinated bovine animals, antibodies against the entire BHV1.
(i) in the case of vaccinated bovine animals, antibodies against the gE-glycoprotein of the BHV1; or
(ii) in the case of unvaccinated bovine animals, antibodies against the entire BHV1.
(a) the animals originate in a Member State listed in Annex I and come from BHV1-free holdings meeting at least the requirements set down in Annex III;
(b) the animals are intended for meat production and comply with the following conditions:(i)the animals either—originate in BHV1-free holdings as defined in Annex III, or—descend from vaccinated and regularly re-vaccinated dams, or—have been regularly vaccinated and re-vaccinated according to the instructions of the manufacturer with a gE-deleted vaccine, or—have been subjected in the Member State of origin with negative result to a serological test for antibodies as referred to in paragraph 1(c) carried out on a sample of blood taken within 14 days of dispatch, and(ii)they are transported without coming into contact with animals of lesser health status to a holding of unknown BHV1-status in the Member State of destination listed in Annex I, where according to the approved national eradication programme all animals are fattened indoors, and from which they can only be transported directly to the slaughterhouse; (i) the animals either—originate in BHV1-free holdings as defined in Annex III, or—descend from vaccinated and regularly re-vaccinated dams, or—have been regularly vaccinated and re-vaccinated according to the instructions of the manufacturer with a gE-deleted vaccine, or—have been subjected in the Member State of origin with negative result to a serological test for antibodies as referred to in paragraph 1(c) carried out on a sample of blood taken within 14 days of dispatch, and — originate in BHV1-free holdings as defined in Annex III, or — descend from vaccinated and regularly re-vaccinated dams, or — have been regularly vaccinated and re-vaccinated according to the instructions of the manufacturer with a gE-deleted vaccine, or — have been subjected in the Member State of origin with negative result to a serological test for antibodies as referred to in paragraph 1(c) carried out on a sample of blood taken within 14 days of dispatch, and (ii) they are transported without coming into contact with animals of lesser health status to a holding of unknown BHV1-status in the Member State of destination listed in Annex I, where according to the approved national eradication programme all animals are fattened indoors, and from which they can only be transported directly to the slaughterhouse;
(i) the animals either—originate in BHV1-free holdings as defined in Annex III, or—descend from vaccinated and regularly re-vaccinated dams, or—have been regularly vaccinated and re-vaccinated according to the instructions of the manufacturer with a gE-deleted vaccine, or—have been subjected in the Member State of origin with negative result to a serological test for antibodies as referred to in paragraph 1(c) carried out on a sample of blood taken within 14 days of dispatch, and — originate in BHV1-free holdings as defined in Annex III, or — descend from vaccinated and regularly re-vaccinated dams, or — have been regularly vaccinated and re-vaccinated according to the instructions of the manufacturer with a gE-deleted vaccine, or — have been subjected in the Member State of origin with negative result to a serological test for antibodies as referred to in paragraph 1(c) carried out on a sample of blood taken within 14 days of dispatch, and
— originate in BHV1-free holdings as defined in Annex III, or
— descend from vaccinated and regularly re-vaccinated dams, or
— have been regularly vaccinated and re-vaccinated according to the instructions of the manufacturer with a gE-deleted vaccine, or
— have been subjected in the Member State of origin with negative result to a serological test for antibodies as referred to in paragraph 1(c) carried out on a sample of blood taken within 14 days of dispatch, and
(ii) they are transported without coming into contact with animals of lesser health status to a holding of unknown BHV1-status in the Member State of destination listed in Annex I, where according to the approved national eradication programme all animals are fattened indoors, and from which they can only be transported directly to the slaughterhouse;
(i) the animals either—originate in BHV1-free holdings as defined in Annex III, or—descend from vaccinated and regularly re-vaccinated dams, or—have been regularly vaccinated and re-vaccinated according to the instructions of the manufacturer with a gE-deleted vaccine, or—have been subjected in the Member State of origin with negative result to a serological test for antibodies as referred to in paragraph 1(c) carried out on a sample of blood taken within 14 days of dispatch, and — originate in BHV1-free holdings as defined in Annex III, or — descend from vaccinated and regularly re-vaccinated dams, or — have been regularly vaccinated and re-vaccinated according to the instructions of the manufacturer with a gE-deleted vaccine, or — have been subjected in the Member State of origin with negative result to a serological test for antibodies as referred to in paragraph 1(c) carried out on a sample of blood taken within 14 days of dispatch, and
— originate in BHV1-free holdings as defined in Annex III, or
— descend from vaccinated and regularly re-vaccinated dams, or
— have been regularly vaccinated and re-vaccinated according to the instructions of the manufacturer with a gE-deleted vaccine, or
— have been subjected in the Member State of origin with negative result to a serological test for antibodies as referred to in paragraph 1(c) carried out on a sample of blood taken within 14 days of dispatch, and
— originate in BHV1-free holdings as defined in Annex III, or
— descend from vaccinated and regularly re-vaccinated dams, or
— have been regularly vaccinated and re-vaccinated according to the instructions of the manufacturer with a gE-deleted vaccine, or
— have been subjected in the Member State of origin with negative result to a serological test for antibodies as referred to in paragraph 1(c) carried out on a sample of blood taken within 14 days of dispatch, and
(ii) they are transported without coming into contact with animals of lesser health status to a holding of unknown BHV1-status in the Member State of destination listed in Annex I, where according to the approved national eradication programme all animals are fattened indoors, and from which they can only be transported directly to the slaughterhouse;
(c) the animals originate from holdings on which all bovine animals on the holding older than 15 months of age have been vaccinated and regularly revaccinated and all animals on the holding older than nine months have been subjected with negative result to a serological test for antibodies against the gE-glycoprotein of the BHV1 at intervals of not more than 12 months and the animals have been tested with negative results for antibodies as referred to in paragraph 1(c)(i) on blood samples taken during the past 14 days prior to dispatch;
(d) the animals originate from BHV1-free holdings as defined in Annex III which are situated in a Member State in which infectious bovine rhinotracheitis is a compulsorily notifiable disease and in which within an area of 5 km radius around the holdings there was no clinical or pathological evidence of BHV1-infection during the past 30 days and the animals have been tested with negative results for antibodies as referred to in paragraph 1(c) on a sample of blood taken during the past 14 days prior to dispatch.
(a) after the first indent: ‘IBR’;
(b) after the second indent: ‘Article 2, paragraph …. point …. of Commission Decision 2004/558/EC’.
(a) they shall comply with the additional guarantees provided for in Article 2(1)(a) and (b);
(b) they and all other bovine animals in the same isolation facility referred to in Article 2(1)(b) must have been subjected with negative results to a serological test carried out on blood samples taken not earlier than 21 days after their arrival at the isolation facility, for the detection of antibodies against the entire BHV1;
(c) they must not have been vaccinated against infectious bovine rhinotracheitis.
(a) after the first indent: ‘IBR’,
(b) after the second indent: ‘Article 3 of Commission Decision 2004/558/EC’.
Member State Regions of Member State to which the additional guarantees for infectious bovine rhinotracheitis apply in accordance with Article 9 of Directive 64/432/EEC
Germany All regions
Member State Regions of Member State to which the additional guarantees for infectious bovine rhinotracheitis apply in accordance with Article 10 of Directive 64/432/EEC
Denmark All regions
Italy Province of Bolzano
Austria All regions
Finland All regions
Sweden All regions
1.1. no suspicion for BHV1 infection has been recorded for the holding during the past six months and all bovine animals on the holding are free from clinical symptoms indicative for BHV1 infection;
1.2. only bovine animals from holdings situated in Member States or regions thereof listed in Annex II or from BHV1-free holdings have been introduced and none of the bovine animals on the holding had contact with bovine animals other than those coming from holdings situated in Member States or regions thereof listed in Annex II or from BHV1-free holdings;
1.3. female bovine animals are only inseminated with semen from bulls produced in accordance with Directive 88/407/EEC and which have been tested with negative result for antibodies as referred to in Article 2(1)(c)(i), or have been serviced by bulls from holdings situated in Member States or regions thereof listed in Annex II or from BHV1-free holdings;
1.4. At least one of the following control regimes is applied on the holding:1.4.1.a serological investigation for antibodies as referred to in Article 2(1)(c) has been carried out with negative results in each case on at least two samples of blood, taken with an interval of five to seven months from all female and male bovine animals used or intended for breeding purposes older than nine months of age;1.4.2.a serological investigation for antibodies against the BHV1 has been carried out with negative result on at least two individual samples of milk, or a pool of milk samples taken from not more than five animals, taken with an interval of five to seven months from all lactating animals, and a serological investigation for antibodies as referred to in Article 2(1)(c) has been carried out with negative results in each case on at least two samples of blood, taken with an interval of five to seven months from all non-lactating female bovine animals and from all male bovine animals used or intended for breeding purposes older than nine months of age;1.4.3.in the case of dairy farms on which at least 30 % of the bovine animals are lactating cows in milk, a serological investigation for antibodies against the BHV1 has been carried out with negative results in each case on at least three milk samples collected, depending on the specification of test employed, from a bulk of not more than 50 animals taken with an interval of at least three months and a serological investigation for antibodies as referred to in Article 2(1)(c) has been carried out with negative results in each case on at least one sample of blood, taken from all non-lactating female bovine animals and from all male bovine animals used or intended for breeding purposes older than nine months of age;1.4.4.all bovine animals on the holding originate either from holdings situated in Member States or regions thereof listed in Annex II or from BHV1-free holdings. 1.4.1. a serological investigation for antibodies as referred to in Article 2(1)(c) has been carried out with negative results in each case on at least two samples of blood, taken with an interval of five to seven months from all female and male bovine animals used or intended for breeding purposes older than nine months of age; 1.4.2. a serological investigation for antibodies against the BHV1 has been carried out with negative result on at least two individual samples of milk, or a pool of milk samples taken from not more than five animals, taken with an interval of five to seven months from all lactating animals, and a serological investigation for antibodies as referred to in Article 2(1)(c) has been carried out with negative results in each case on at least two samples of blood, taken with an interval of five to seven months from all non-lactating female bovine animals and from all male bovine animals used or intended for breeding purposes older than nine months of age; 1.4.3. in the case of dairy farms on which at least 30 % of the bovine animals are lactating cows in milk, a serological investigation for antibodies against the BHV1 has been carried out with negative results in each case on at least three milk samples collected, depending on the specification of test employed, from a bulk of not more than 50 animals taken with an interval of at least three months and a serological investigation for antibodies as referred to in Article 2(1)(c) has been carried out with negative results in each case on at least one sample of blood, taken from all non-lactating female bovine animals and from all male bovine animals used or intended for breeding purposes older than nine months of age; 1.4.4. all bovine animals on the holding originate either from holdings situated in Member States or regions thereof listed in Annex II or from BHV1-free holdings.
1.4.1. a serological investigation for antibodies as referred to in Article 2(1)(c) has been carried out with negative results in each case on at least two samples of blood, taken with an interval of five to seven months from all female and male bovine animals used or intended for breeding purposes older than nine months of age;
1.4.2. a serological investigation for antibodies against the BHV1 has been carried out with negative result on at least two individual samples of milk, or a pool of milk samples taken from not more than five animals, taken with an interval of five to seven months from all lactating animals, and a serological investigation for antibodies as referred to in Article 2(1)(c) has been carried out with negative results in each case on at least two samples of blood, taken with an interval of five to seven months from all non-lactating female bovine animals and from all male bovine animals used or intended for breeding purposes older than nine months of age;
1.4.3. in the case of dairy farms on which at least 30 % of the bovine animals are lactating cows in milk, a serological investigation for antibodies against the BHV1 has been carried out with negative results in each case on at least three milk samples collected, depending on the specification of test employed, from a bulk of not more than 50 animals taken with an interval of at least three months and a serological investigation for antibodies as referred to in Article 2(1)(c) has been carried out with negative results in each case on at least one sample of blood, taken from all non-lactating female bovine animals and from all male bovine animals used or intended for breeding purposes older than nine months of age;
1.4.4. all bovine animals on the holding originate either from holdings situated in Member States or regions thereof listed in Annex II or from BHV1-free holdings.
1.4.1. a serological investigation for antibodies as referred to in Article 2(1)(c) has been carried out with negative results in each case on at least two samples of blood, taken with an interval of five to seven months from all female and male bovine animals used or intended for breeding purposes older than nine months of age;
1.4.2. a serological investigation for antibodies against the BHV1 has been carried out with negative result on at least two individual samples of milk, or a pool of milk samples taken from not more than five animals, taken with an interval of five to seven months from all lactating animals, and a serological investigation for antibodies as referred to in Article 2(1)(c) has been carried out with negative results in each case on at least two samples of blood, taken with an interval of five to seven months from all non-lactating female bovine animals and from all male bovine animals used or intended for breeding purposes older than nine months of age;
1.4.3. in the case of dairy farms on which at least 30 % of the bovine animals are lactating cows in milk, a serological investigation for antibodies against the BHV1 has been carried out with negative results in each case on at least three milk samples collected, depending on the specification of test employed, from a bulk of not more than 50 animals taken with an interval of at least three months and a serological investigation for antibodies as referred to in Article 2(1)(c) has been carried out with negative results in each case on at least one sample of blood, taken from all non-lactating female bovine animals and from all male bovine animals used or intended for breeding purposes older than nine months of age;
1.4.4. all bovine animals on the holding originate either from holdings situated in Member States or regions thereof listed in Annex II or from BHV1-free holdings.
2.1. the conditions in paragraphs 1.1 to 1.3 continue to apply; and
2.2. at least one of the following control regimes is applied:2.2.1.all bovine animals on the holding older than 24 months of age have reacted with negative result to a serological test for the detection of antibodies as referred to in Article 2(1)(c) carried out on a sample of blood taken at intervals of not more than 12 months;2.2.2.the serological investigation for antibodies against the BHV1 has been carried out with negative result on at least one individual sample of milk, or a pool of milk samples taken from not more than five animals, taken at intervals of not more than 12 months from all lactating animals, and all non-lactating female bovine animals and male bovine animals on the holding older than 24 months of age have reacted with negative result to a serological test for the detection of antibodies as referred to in Article 2(1)(c) carried out on a sample of blood taken at intervals of not more than 12 months;2.2.3.in the case of dairy farms on which at least 30 % of the bovine animals are lactating cows in milk, the serological investigation for antibodies against the BHV1 has been carried out with negative result on at least two milk samples collected, depending on the specification of test employed, from a bulk of not more than 50 animals taken at intervals of at least three months and not more than 12 months and a serological investigation for antibodies as referred to in Article 2(1)(c) has been carried out with negative results in each case on at least one sample of blood, taken from all non-lactating female bovine animals and male bovine animals older than 24 months of age at intervals of not more than 12 months. 2.2.1. all bovine animals on the holding older than 24 months of age have reacted with negative result to a serological test for the detection of antibodies as referred to in Article 2(1)(c) carried out on a sample of blood taken at intervals of not more than 12 months; 2.2.2. the serological investigation for antibodies against the BHV1 has been carried out with negative result on at least one individual sample of milk, or a pool of milk samples taken from not more than five animals, taken at intervals of not more than 12 months from all lactating animals, and all non-lactating female bovine animals and male bovine animals on the holding older than 24 months of age have reacted with negative result to a serological test for the detection of antibodies as referred to in Article 2(1)(c) carried out on a sample of blood taken at intervals of not more than 12 months; 2.2.3. in the case of dairy farms on which at least 30 % of the bovine animals are lactating cows in milk, the serological investigation for antibodies against the BHV1 has been carried out with negative result on at least two milk samples collected, depending on the specification of test employed, from a bulk of not more than 50 animals taken at intervals of at least three months and not more than 12 months and a serological investigation for antibodies as referred to in Article 2(1)(c) has been carried out with negative results in each case on at least one sample of blood, taken from all non-lactating female bovine animals and male bovine animals older than 24 months of age at intervals of not more than 12 months.
2.2.1. all bovine animals on the holding older than 24 months of age have reacted with negative result to a serological test for the detection of antibodies as referred to in Article 2(1)(c) carried out on a sample of blood taken at intervals of not more than 12 months;
2.2.2. the serological investigation for antibodies against the BHV1 has been carried out with negative result on at least one individual sample of milk, or a pool of milk samples taken from not more than five animals, taken at intervals of not more than 12 months from all lactating animals, and all non-lactating female bovine animals and male bovine animals on the holding older than 24 months of age have reacted with negative result to a serological test for the detection of antibodies as referred to in Article 2(1)(c) carried out on a sample of blood taken at intervals of not more than 12 months;
2.2.3. in the case of dairy farms on which at least 30 % of the bovine animals are lactating cows in milk, the serological investigation for antibodies against the BHV1 has been carried out with negative result on at least two milk samples collected, depending on the specification of test employed, from a bulk of not more than 50 animals taken at intervals of at least three months and not more than 12 months and a serological investigation for antibodies as referred to in Article 2(1)(c) has been carried out with negative results in each case on at least one sample of blood, taken from all non-lactating female bovine animals and male bovine animals older than 24 months of age at intervals of not more than 12 months.
2.2.1. all bovine animals on the holding older than 24 months of age have reacted with negative result to a serological test for the detection of antibodies as referred to in Article 2(1)(c) carried out on a sample of blood taken at intervals of not more than 12 months;
2.2.2. the serological investigation for antibodies against the BHV1 has been carried out with negative result on at least one individual sample of milk, or a pool of milk samples taken from not more than five animals, taken at intervals of not more than 12 months from all lactating animals, and all non-lactating female bovine animals and male bovine animals on the holding older than 24 months of age have reacted with negative result to a serological test for the detection of antibodies as referred to in Article 2(1)(c) carried out on a sample of blood taken at intervals of not more than 12 months;
2.2.3. in the case of dairy farms on which at least 30 % of the bovine animals are lactating cows in milk, the serological investigation for antibodies against the BHV1 has been carried out with negative result on at least two milk samples collected, depending on the specification of test employed, from a bulk of not more than 50 animals taken at intervals of at least three months and not more than 12 months and a serological investigation for antibodies as referred to in Article 2(1)(c) has been carried out with negative results in each case on at least one sample of blood, taken from all non-lactating female bovine animals and male bovine animals older than 24 months of age at intervals of not more than 12 months.
THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Council Directive 64/432/EEC of 26 June 1964 on animal health problems affecting intra-Community trade in bovine animals and swine(1), and in particular Articles 9(2) and 10(2) thereof,
(1) Infectious bovine rhinotracheitis is the description of the most prominent clinical signs of the infection with the bovine herpesvirus type 1 (BHV1). As many infections with that virus run a subclinical course, control measures should be directed to the eradication of the infection rather than to the suppression of symptoms.
(2) Annex E (II) to Directive 64/432/EEC lists ‘infectious bovine rhinotracheitis’ among the diseases for which national control programmes may be approved and additional guarantees requested.
(3) Germany had submitted a programme conducted with the aim of eradicating the BHV1 infection in all parts of its territory, which complies with the criteria set out in Article 9(1) of Directive 64/432/EEC and provides for rules for the national movement of bovine animals which are equivalent to those previously implemented in Austria, the Province of Bolzano in Italy and Sweden which were successful in eradicating the disease from those countries.
(4) The programme presented by Germany and, as requested by that Member State, the additional guarantees in relation to trade in bovine animals in order to secure the success of that programme were approved by Decision 2004/215/EC of 1 March 2004 implementing Council Directive 64/432/EEC as regards additional guarantees for intra-Community trade in bovine animals relating to infectious bovine rhinotracheitis and the approval of the eradication programmes presented by certain Member States(2).
(5) Additional guarantees exist as regards Denmark, Austria, Finland and Sweden as well as Italy, concerning the province of Bolzano. Those Member States consider that their territory is free from infectious bovine rhinotracheitis and Italy takes the same view for the Province of Bolzano. In accordance with Article 10(1) of Directive 64/432/EEC, they submitted supporting documentation to the Commission, in particular substantiating that monitoring of the situation is continued.
(6) To Member States or regions thereof that are recognised as being free of that disease and which are currently listed in the Annex to Commission Decision 93/42/EEC(3)only minimum requirements for the dispatch of bovine animals for breeding and production to other Member States should apply.
(7) For the standardisation of BHV1 tests in laboratories the World Organisation for Animal Health (OIE) has adopted a strong positive, a weak positive and negative serum as OIE international standards for BHV1 tests which are available at the OIE Reference Laboratories for infectious bovine rhinotracheitis mentioned in the Manual of Standards for Diagnostic Tests and Vaccines(4).
(8) Problems have been encountered in relation to intra-Community trade in bovine animals originating in Member States of different status with regard to infectious bovine rhinotracheitis.
(9) For reasons of clarity and in order to ensure the linguistic consistency of the measures, it is appropriate to combine in a single Decision the approval of the German programme and the additional guarantees for infectious bovine rhinotracheitis and to repeal Decision 2004/215/EC.
(10) The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health,
HAS ADOPTED THIS DECISION:

Article 1
The programmes presented by the Member States listed in the first column of the table in Annex I for the control and eradication of the infection with the bovine herpesvirus type 1 (BHV1), hereinafter referred to as ‘infectious bovine rhinotracheitis’ or ‘IBR’, in regions of these Member States specified in the second column of the table in Annex I are approved.

Article 2
1. Bovine animals for breeding and production coming from Member States or regions thereof other than those listed in Annex II and destined for Member States or regions thereof listed in Annex I, shall meet at least the following additional guarantees:
(a)
they must come from a holding on which, according to official information, no clinical or pathological evidence of infectious bovine rhinotracheitis has been recorded for the past 12 months;
(b)
they must have been isolated in a facility approved by the competent authority for 30 days immediately prior to movement and all bovine animals in the same isolation facility must have remained free of clinical signs of infectious bovine rhinotracheitis during that period;
(c)
they and all other bovine animals in the same isolation facility must have been subjected with negative results to a serological test carried out on blood samples, taken not earlier than 21 days after their arrival at the isolation facility, for the detection of the following antibodies:
(i)
in the case of vaccinated bovine animals, antibodies against the gE-glycoprotein of the BHV1; or
(ii)
in the case of unvaccinated bovine animals, antibodies against the entire BHV1.
2. By way of derogation to paragraph 1, the competent authorities of the Member State of origin may authorise the dispatch to holdings situated in regions listed in Annex I of bovine animals complying with at least one of the following alternative conditions:
(a)
the animals originate in a Member State listed in Annex I and come from BHV1-free holdings meeting at least the requirements set down in Annex III;
(b)
the animals are intended for meat production and comply with the following conditions:
(i)
the animals either
—
originate in BHV1-free holdings as defined in Annex III, or
—
descend from vaccinated and regularly re-vaccinated dams, or
—
have been regularly vaccinated and re-vaccinated according to the instructions of the manufacturer with a gE-deleted vaccine, or
—
have been subjected in the Member State of origin with negative result to a serological test for antibodies as referred to in paragraph 1(c) carried out on a sample of blood taken within 14 days of dispatch, and
(ii)
they are transported without coming into contact with animals of lesser health status to a holding of unknown BHV1-status in the Member State of destination listed in Annex I, where according to the approved national eradication programme all animals are fattened indoors, and from which they can only be transported directly to the slaughterhouse;
(c)
the animals originate from holdings on which all bovine animals on the holding older than 15 months of age have been vaccinated and regularly revaccinated and all animals on the holding older than nine months have been subjected with negative result to a serological test for antibodies against the gE-glycoprotein of the BHV1 at intervals of not more than 12 months and the animals have been tested with negative results for antibodies as referred to in paragraph 1(c)(i) on blood samples taken during the past 14 days prior to dispatch;
(d)
the animals originate from BHV1-free holdings as defined in Annex III which are situated in a Member State in which infectious bovine rhinotracheitis is a compulsorily notifiable disease and in which within an area of 5 km radius around the holdings there was no clinical or pathological evidence of BHV1-infection during the past 30 days and the animals have been tested with negative results for antibodies as referred to in paragraph 1(c) on a sample of blood taken during the past 14 days prior to dispatch.
3. Bovine animals for slaughter coming from Member States or regions thereof other than those listed in Annex II and destined for Member States or regions thereof listed in Annex I shall be transported directly to the slaughterhouse of destination or to an approved assembly centre from where they shall be removed in accordance with Article 7, second indent, of Directive 64/432/EEC to the slaughterhouse to be slaughtered.
4. In point 4 of Section C of the health certificate set out in Model 1 of Annex F to Directive 64/432/EEC accompanying bovine animals as referred to in paragraph 1, the following information shall be inserted:
(a)
after the first indent: ‘IBR’;
(b)
after the second indent: ‘Article 2, paragraph …. point …. of Commission Decision 2004/558/EC’.

Article 3
1. Bovine animals for breeding and production coming from Member States or regions thereof other than those listed in Annex II and destined for Member States or regions thereof free of infectious bovine rhinotracheitis and listed in Annex II, shall meet the following additional guarantees:
(a)
they shall comply with the additional guarantees provided for in Article 2(1)(a) and (b);
(b)
they and all other bovine animals in the same isolation facility referred to in Article 2(1)(b) must have been subjected with negative results to a serological test carried out on blood samples taken not earlier than 21 days after their arrival at the isolation facility, for the detection of antibodies against the entire BHV1;
(c)
they must not have been vaccinated against infectious bovine rhinotracheitis.
2. Bovine animals for slaughter coming from Member States or regions thereof other than those listed in Annex II and destined for Member States or regions thereof listed in Annex II shall be transported directly to the slaughterhouse of destination to be slaughtered in accordance with Article 7, first indent, of Directive 64/432/EEC.
3. In point 4 of Section C of the health certificate set out in Model 1 of Annex F to Directive 64/432/EEC accompanying bovine animals as referred to in paragraph 1, the following information shall be inserted:
(a)
after the first indent: ‘IBR’,
(b)
after the second indent: ‘Article 3 of Commission Decision 2004/558/EC’.

Article 4
Bovine animals for breeding and production originating in a Member State or region thereof listed in Annex II and destined for a Member State or region thereof listed in Annexes I or II shall comply with the conditions provided for in Article 2(1)(a).

Article 5
Member States shall ensure that the serological test referred to in Article 2(1)(c)(ii) and in Article 3(1)(b) for the detection of antibodies against the entire BHV1 is standardised against the strong positive, weak positive and negative serum adopted as OIE international standards for BHV1 tests.

Article 6
Decision 2004/215/EC is repealed.

Article 7
This Decision shall apply from 26 July 2004.

Article 8
This Decision is addressed to the Member States.

THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Council Directive 64/432/EEC of 26 June 1964 on animal health problems affecting intra-Community trade in bovine animals and swine(1), and in particular Articles 9(2) and 10(2) thereof,
(1) Infectious bovine rhinotracheitis is the description of the most prominent clinical signs of the infection with the bovine herpesvirus type 1 (BHV1). As many infections with that virus run a subclinical course, control measures should be directed to the eradication of the infection rather than to the suppression of symptoms.
(2) Annex E (II) to Directive 64/432/EEC lists ‘infectious bovine rhinotracheitis’ among the diseases for which national control programmes may be approved and additional guarantees requested.
(3) Germany had submitted a programme conducted with the aim of eradicating the BHV1 infection in all parts of its territory, which complies with the criteria set out in Article 9(1) of Directive 64/432/EEC and provides for rules for the national movement of bovine animals which are equivalent to those previously implemented in Austria, the Province of Bolzano in Italy and Sweden which were successful in eradicating the disease from those countries.
(4) The programme presented by Germany and, as requested by that Member State, the additional guarantees in relation to trade in bovine animals in order to secure the success of that programme were approved by Decision 2004/215/EC of 1 March 2004 implementing Council Directive 64/432/EEC as regards additional guarantees for intra-Community trade in bovine animals relating to infectious bovine rhinotracheitis and the approval of the eradication programmes presented by certain Member States(2).
(5) Additional guarantees exist as regards Denmark, Austria, Finland and Sweden as well as Italy, concerning the province of Bolzano. Those Member States consider that their territory is free from infectious bovine rhinotracheitis and Italy takes the same view for the Province of Bolzano. In accordance with Article 10(1) of Directive 64/432/EEC, they submitted supporting documentation to the Commission, in particular substantiating that monitoring of the situation is continued.
(6) To Member States or regions thereof that are recognised as being free of that disease and which are currently listed in the Annex to Commission Decision 93/42/EEC(3)only minimum requirements for the dispatch of bovine animals for breeding and production to other Member States should apply.
(7) For the standardisation of BHV1 tests in laboratories the World Organisation for Animal Health (OIE) has adopted a strong positive, a weak positive and negative serum as OIE international standards for BHV1 tests which are available at the OIE Reference Laboratories for infectious bovine rhinotracheitis mentioned in the Manual of Standards for Diagnostic Tests and Vaccines(4).
(8) Problems have been encountered in relation to intra-Community trade in bovine animals originating in Member States of different status with regard to infectious bovine rhinotracheitis.
(9) For reasons of clarity and in order to ensure the linguistic consistency of the measures, it is appropriate to combine in a single Decision the approval of the German programme and the additional guarantees for infectious bovine rhinotracheitis and to repeal Decision 2004/215/EC.
(10) The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health,
HAS ADOPTED THIS DECISION:
The programmes presented by the Member States listed in the first column of the table in Annex I for the control and eradication of the infection with the bovine herpesvirus type 1 (BHV1), hereinafter referred to as ‘infectious bovine rhinotracheitis’ or ‘IBR’, in regions of these Member States specified in the second column of the table in Annex I are approved.
1. Bovine animals for breeding and production coming from Member States or regions thereof other than those listed in Annex II and destined for Member States or regions thereof listed in Annex I, shall meet at least the following additional guarantees:
(a)
they must come from a holding on which, according to official information, no clinical or pathological evidence of infectious bovine rhinotracheitis has been recorded for the past 12 months;
(b)
they must have been isolated in a facility approved by the competent authority for 30 days immediately prior to movement and all bovine animals in the same isolation facility must have remained free of clinical signs of infectious bovine rhinotracheitis during that period;
(c)
they and all other bovine animals in the same isolation facility must have been subjected with negative results to a serological test carried out on blood samples, taken not earlier than 21 days after their arrival at the isolation facility, for the detection of the following antibodies:
(i)
in the case of vaccinated bovine animals, antibodies against the gE-glycoprotein of the BHV1; or
(ii)
in the case of unvaccinated bovine animals, antibodies against the entire BHV1.
2. By way of derogation to paragraph 1, the competent authorities of the Member State of origin may authorise the dispatch to holdings situated in regions listed in Annex I of bovine animals complying with at least one of the following alternative conditions:
(a)
the animals originate in a Member State listed in Annex I and come from BHV1-free holdings meeting at least the requirements set down in Annex III;
(b)
the animals are intended for meat production and comply with the following conditions:
(i)
the animals either
—
originate in BHV1-free holdings as defined in Annex III, or
—
descend from vaccinated and regularly re-vaccinated dams, or
—
have been regularly vaccinated and re-vaccinated according to the instructions of the manufacturer with a gE-deleted vaccine, or
—
have been subjected in the Member State of origin with negative result to a serological test for antibodies as referred to in paragraph 1(c) carried out on a sample of blood taken within 14 days of dispatch, and
(ii)
they are transported without coming into contact with animals of lesser health status to a holding of unknown BHV1-status in the Member State of destination listed in Annex I, where according to the approved national eradication programme all animals are fattened indoors, and from which they can only be transported directly to the slaughterhouse;
(c)
the animals originate from holdings on which all bovine animals on the holding older than 15 months of age have been vaccinated and regularly revaccinated and all animals on the holding older than nine months have been subjected with negative result to a serological test for antibodies against the gE-glycoprotein of the BHV1 at intervals of not more than 12 months and the animals have been tested with negative results for antibodies as referred to in paragraph 1(c)(i) on blood samples taken during the past 14 days prior to dispatch;
(d)
the animals originate from BHV1-free holdings as defined in Annex III which are situated in a Member State in which infectious bovine rhinotracheitis is a compulsorily notifiable disease and in which within an area of 5 km radius around the holdings there was no clinical or pathological evidence of BHV1-infection during the past 30 days and the animals have been tested with negative results for antibodies as referred to in paragraph 1(c) on a sample of blood taken during the past 14 days prior to dispatch.
3. Bovine animals for slaughter coming from Member States or regions thereof other than those listed in Annex II and destined for Member States or regions thereof listed in Annex I shall be transported directly to the slaughterhouse of destination or to an approved assembly centre from where they shall be removed in accordance with Article 7, second indent, of Directive 64/432/EEC to the slaughterhouse to be slaughtered.
4. In point 4 of Section C of the health certificate set out in Model 1 of Annex F to Directive 64/432/EEC accompanying bovine animals as referred to in paragraph 1, the following information shall be inserted:
(a)
after the first indent: ‘IBR’;
(b)
after the second indent: ‘Article 2, paragraph …. point …. of Commission Decision 2004/558/EC’.
1. Bovine animals for breeding and production coming from Member States or regions thereof other than those listed in Annex II and destined for Member States or regions thereof free of infectious bovine rhinotracheitis and listed in Annex II, shall meet the following additional guarantees:
(a)
they shall comply with the additional guarantees provided for in Article 2(1)(a) and (b);
(b)
they and all other bovine animals in the same isolation facility referred to in Article 2(1)(b) must have been subjected with negative results to a serological test carried out on blood samples taken not earlier than 21 days after their arrival at the isolation facility, for the detection of antibodies against the entire BHV1;
(c)
they must not have been vaccinated against infectious bovine rhinotracheitis.
2. Bovine animals for slaughter coming from Member States or regions thereof other than those listed in Annex II and destined for Member States or regions thereof listed in Annex II shall be transported directly to the slaughterhouse of destination to be slaughtered in accordance with Article 7, first indent, of Directive 64/432/EEC.
3. In point 4 of Section C of the health certificate set out in Model 1 of Annex F to Directive 64/432/EEC accompanying bovine animals as referred to in paragraph 1, the following information shall be inserted:
(a)
after the first indent: ‘IBR’,
(b)
after the second indent: ‘Article 3 of Commission Decision 2004/558/EC’.
Bovine animals for breeding and production originating in a Member State or region thereof listed in Annex II and destined for a Member State or region thereof listed in Annexes I or II shall comply with the conditions provided for in Article 2(1)(a).
Member States shall ensure that the serological test referred to in Article 2(1)(c)(ii) and in Article 3(1)(b) for the detection of antibodies against the entire BHV1 is standardised against the strong positive, weak positive and negative serum adopted as OIE international standards for BHV1 tests.
Decision 2004/215/EC is repealed.
This Decision shall apply from 26 July 2004.
This Decision is addressed to the Member States.
ANNEX I
Member State | Regions of Member State to which the additional guarantees for infectious bovine rhinotracheitis apply in accordance with Article 9 of Directive 64/432/EEC
Germany | All regions
ANNEX II
Member State | Regions of Member State to which the additional guarantees for infectious bovine rhinotracheitis apply in accordance with Article 10 of Directive 64/432/EEC
Denmark | All regions
Italy | Province of Bolzano
Austria | All regions
Finland | All regions
Sweden | All regions
ANNEX IIIBHV1-free holding 1.
A holding keeping bovine animals shall be considered free of BHV1 infection if it complies with the following conditions:
1.1. no suspicion for BHV1 infection has been recorded for the holding during the past six months and all bovine animals on the holding are free from clinical symptoms indicative for BHV1 infection;
1.2. only bovine animals from holdings situated in Member States or regions thereof listed in Annex II or from BHV1-free holdings have been introduced and none of the bovine animals on the holding had contact with bovine animals other than those coming from holdings situated in Member States or regions thereof listed in Annex II or from BHV1-free holdings;
1.3. female bovine animals are only inseminated with semen from bulls produced in accordance with Directive 88/407/EEC and which have been tested with negative result for antibodies as referred to in Article 2(1)(c)(i), or have been serviced by bulls from holdings situated in Member States or regions thereof listed in Annex II or from BHV1-free holdings;
1.4. At least one of the following control regimes is applied on the holding:
1.4.1. a serological investigation for antibodies as referred to in Article 2(1)(c) has been carried out with negative results in each case on at least two samples of blood, taken with an interval of five to seven months from all female and male bovine animals used or intended for breeding purposes older than nine months of age;
1.4.2. a serological investigation for antibodies against the BHV1 has been carried out with negative result on at least two individual samples of milk, or a pool of milk samples taken from not more than five animals, taken with an interval of five to seven months from all lactating animals, and a serological investigation for antibodies as referred to in Article 2(1)(c) has been carried out with negative results in each case on at least two samples of blood, taken with an interval of five to seven months from all non-lactating female bovine animals and from all male bovine animals used or intended for breeding purposes older than nine months of age;
1.4.3. in the case of dairy farms on which at least 30 % of the bovine animals are lactating cows in milk, a serological investigation for antibodies against the BHV1 has been carried out with negative results in each case on at least three milk samples collected, depending on the specification of test employed, from a bulk of not more than 50 animals taken with an interval of at least three months and a serological investigation for antibodies as referred to in Article 2(1)(c) has been carried out with negative results in each case on at least one sample of blood, taken from all non-lactating female bovine animals and from all male bovine animals used or intended for breeding purposes older than nine months of age;
1.4.4. all bovine animals on the holding originate either from holdings situated in Member States or regions thereof listed in Annex II or from BHV1-free holdings.
2.
The BHV1-free status of a holding keeping bovine animals is retained if:
2.1. the conditions in paragraphs 1.1 to 1.3 continue to apply; and
2.2. at least one of the following control regimes is applied:
2.2.1. all bovine animals on the holding older than 24 months of age have reacted with negative result to a serological test for the detection of antibodies as referred to in Article 2(1)(c) carried out on a sample of blood taken at intervals of not more than 12 months;
2.2.2. the serological investigation for antibodies against the BHV1 has been carried out with negative result on at least one individual sample of milk, or a pool of milk samples taken from not more than five animals, taken at intervals of not more than 12 months from all lactating animals, and all non-lactating female bovine animals and male bovine animals on the holding older than 24 months of age have reacted with negative result to a serological test for the detection of antibodies as referred to in Article 2(1)(c) carried out on a sample of blood taken at intervals of not more than 12 months;
2.2.3. in the case of dairy farms on which at least 30 % of the bovine animals are lactating cows in milk, the serological investigation for antibodies against the BHV1 has been carried out with negative result on at least two milk samples collected, depending on the specification of test employed, from a bulk of not more than 50 animals taken at intervals of at least three months and not more than 12 months and a serological investigation for antibodies as referred to in Article 2(1)(c) has been carried out with negative results in each case on at least one sample of blood, taken from all non-lactating female bovine animals and male bovine animals older than 24 months of age at intervals of not more than 12 months.
3.
The BHV1-free status of a holding keeping bovine animals is suspended where during the investigations referred to in paragraph 2.2.1. to 2.2.3. an animal reacted with positive result in a test for antibodies as referred to in Article 2(1)(c);
4.
The BHV1-free status suspended in accordance with paragraph 3 shall only be restored after a serological investigation has been carried out with negative result in each case on two occasions with an interval of at least two months and commencing not earlier than 30 days after the removal of the seropositive animals which includes serological testing for antibodies as referred to in Article 2(1)(c) of all bovine animals on the holding carried out on samples of blood, or in the case of lactating cows, testing for antibodies against the BHV1 carried out on individual milk samples, or pools of milk samples taken from not more than five animals.