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Council Directive 92/65/EECShow full title
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
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Revised version PDFs
- Revised 16/07/20192.07 MB
- Revised 22/11/20171.80 MB
- Revised 29/12/20141.34 MB
- Revised 18/07/20130.72 MB
- Revised 01/03/20120.71 MB
- Revised 11/11/20100.69 MB
- Revised 01/09/20100.44 MB
- Revised 03/09/20080.39 MB
- Revised 01/05/20070.29 MB
- Revised 03/07/20040.32 MB
- Revised 20/05/20040.39 MB
- Revised 01/05/20040.30 MB
- Revised 26/08/20030.31 MB
- Revised 01/03/20030.31 MB
- Revised 31/07/20010.15 MB
- Revised 01/10/19950.15 MB
- Revised 01/01/19950.15 MB
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Changes over time for: Article 13
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Article 13U.K.
1.Trade in animals of species susceptible to the diseases listed in Annex A or to the diseases listed in Annex B, where the Member State of destination applies the guarantee provided for in Articles 14 and 15, and trade in semen, ova or embryos of such animals consigned to and from bodies, institutes or centres approved in accordance with Annex C shall be subject to production of a transport document corresponding to the specimen in Annex E. This document, which must be completed by the veterinarian responsible for the body, institute or centre of origin, must specify that the animals, semen, ova or embryos come from a body, institute or centre approved in accordance with Annex C and must accompany them during transport.
2.(a)To be approved, bodies, institutes or centres shall, as regards notifiable diseases, submit to the competent authority of the Member State all relevant supporting documents relating to the requirements contained in Annex C.
(b)After receiving the file relating to the request for approval or for renewal of approval, the competent authority shall examine it in the light of the information it contains and, where appropriate, of the results of the tests conducted on the spot.
(c)The competent authority shall withdraw approval in accordance with point 3 of Annex C.
[F1(d) All approved bodies, institutes and centres shall be registered and issued with an approval number by the competent authority.
Each Member State shall draw up and keep up to date a list of approved bodies, institutes and centres and their approval numbers and shall make it available to the other Member States and to the public.
Detailed rules for the uniform application of this point may be adopted in accordance with the procedure referred to in Article 26.]
[F2 [F3(e) Sweden shall have a period of two years from the date of entry into force of the Accession Treaty to implement the measures laid down regarding bodies, institutes and centres.] ]
Textual Amendments
F1 Substituted by Council Directive 2008/73/EC of 15 July 2008 simplifying procedures of listing and publishing information in the veterinary and zootechnical fields and amending Directives 64/432/EEC, 77/504/EEC, 88/407/EEC, 88/661/EEC, 89/361/EEC, 89/556/EEC, 90/426/EEC, 90/427/EEC, 90/428/EEC, 90/429/EEC, 90/539/EEC, 91/68/EEC, 91/496/EEC, 92/35/EEC, 92/65/EEC, 92/66/EEC, 92/119/EEC, 94/28/EC, 2000/75/EC, Decision 2000/258/EC and Directives 2001/89/EC, 2002/60/EC and 2005/94/EC (Text with EEA relevance).
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