- Y Diweddaraf sydd Ar Gael (Diwygiedig)
- Pwynt Penodol mewn Amser (01/07/2008)
- Gwreiddiol (Fel y’i mabwysiadwyd gan yr UE)
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Council of 3 October 2002 laying down health rules concerning animal by-products not intended for human consumption (repealed)
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Version Superseded: 04/03/2011
Point in time view as at 01/07/2008.
There are currently no known outstanding effects by UK legislation for Regulation (EC) No 1774/2002 of the European Parliament and of the Council (repealed), ANNEX II.
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Category 1, Category 2 and Category 3 materials are identifiable and kept separate and identifiable during collection and transportation;
processed products are identifiable and kept separate and identifiable during transportation;
a marking substance for the identification of animal by-products or processed products of a specific category is only used for the category for which its use is required under this Regulation, or is established or laid down pursuant to point 4; and
animal by-products and processed products are dispatched from one Member State to another Member State in packaging, containers or vehicles which are prominently and, at least for the period of transport, indelibly colour-coded as follows:
in the case of Category 1 materials, using the colour black;
in the case of Category 2 materials (other than manure and digestive tract content), using the colour yellow;
in the case of Category 3 materials, using the colour green with a high content of blue to ensure that it is clearly distinguishable from the other colours.
clearly indicate the category of the animal by-products or, in the case of processed products, the category of animal by-products from which the processed products were derived; and
bear the following words:
in the case of Category 3 material, ‘ not for human consumption ’ ;
in the case of Category 2 material (other than manure and digestive tract content) and processed products derived therefrom, ‘ not for animal consumption ’ ; however, when Category 2 material is intended for the feeding of animals referred to in Article 23(2)(c) under the conditions provided for in that Article, the label shall instead indicate ‘ for feeding to … ’ completed with the name of the specific species of those animals for the feeding of which the material is intended;
in the case of Category 1 material and processed products derived therefrom, ‘ for disposal only ’ ;
in the case of manure and digestive tract content, ‘ manure ’ .
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cleaned, washed and disinfected after each use;
maintained in a clean condition; and
clean and dry before use.
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the date on which the material was taken from the premises;
the description of the material, including the information referred to in Chapter I, the animal species for Category 3 material and processed products derived therefrom destined for use as feed material and, if applicable, the ear-tag number;
the quantity of the material;
the place of origin of the material;
the name and the address of the carrier;
the name and the address of the receiver and, if applicable, its approval number; and
if appropriate:
the approval number of the plant of origin, and
the nature and the methods of the treatment.
The records referred to in Article 9 must contain the information referred to in Chapter III, paragraph 2, as follows. They must contain:
the information referred to in subparagraphs (b) and (c); and
in the case of records kept by any person consigning animal by-products, the information referred to in subparagraphs (a), (e) and, if known, (f); or
in the case of records kept by any person transporting animal by-products, the information referred to in subparagraphs (a), (d) and (f); or
in the case of records kept by any person receiving animal by-products, the date of reception and the information referred to in subparagraphs (d) and (e).
The commercial document and the health certificate referred to in Chapter III, and the records referred to in Chapter IV, must be kept for a period of at least two years for presentation to the competent authority.
The carriage of animal by-products and processed products in transit must meet the requirements of Chapters I, II, III and VI.
The competent authority must take the necessary measures to control the collection, transport, use and disposal of animal by-products and processed products, including by checking the keeping of required records and documents and, when this Regulation requires it or the competent authority considers it necessary, by sealing.
When the competent authority applies a seal to a consignment of animal by-products or processed products, it must inform the competent authority of the place of destination.
[F1A commercial document in accordance with the model set out in this Chapter shall accompany animal by-products and processed products during transportation. However, for the transport of animal by-products and processed products on their own territory Member States may require:
to use a different commercial document, in paper or in electronic form, provided that such commercial document complies with the requirements laid down in point 2 of Chapter III;
that the quantity of the material referred to in point 2(c) of Chapter III is expressed in weight of the material in the commercial document;
that a copy of the commercial document is returned by the receiver to the producer to be kept by that producer in accordance with Chapter V as proof of arrival of the consignment.]
Where more than one transporter is involved, each transporter shall fill in a declaration as referred to in point 7 of the commercial document, which shall be part of the document.
the date on which the material was taken from the premises;
the description of the material, including the identification of the material, the animal species for Category 3 material and processed products derived therefrom destined for use as feed material and, if applicable, the ear-tag number of the animal;
the quantity of the material;
the place of origin of the material;
the name and the address of the carrier of the material;
the name and the address of the receiver and, if applicable, its approval number; and
if appropriate, the approval number of the plant of origin, and the nature and the methods of the treatment.
Textual Amendments
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