Commission Regulation (EU) No 206/2010Show full title

Commission Regulation (EU) No 206/2010 of 12 March 2010 laying down lists of third countries, territories or parts thereof authorised for the introduction into the European Union of certain animals and fresh meat and the veterinary certification requirements (Text with EEA relevance)

  1. Introductory Text

  2. CHAPTER I SUBJECT MATTER, SCOPE AND DEFINITIONS

    1. Article 1. Subject matter and scope

    2. Article 2. Definitions

    3. Article 2a.Publication of code representing country or part thereof

    4. Article 2b.Publication of closing date and opening date

    5. Article 2c.Specific conditions – live ungulates and fresh meat

    6. Article 2d.Supplementary guarantees – live ungulates

  3. CHAPTER II CONDITIONS FOR THE INTRODUCTION OF LIVE ANIMALS INTO GREAT BRITAIN

    1. Article 3. General conditions for the introduction of ungulates into Great Britain

    2. Article 3a. Conditions for the introduction of ungulates intended for an approved body, institute or centre

    3. Article 3b.Conditions for the entry and transit of ungulates intended for an approved body, institute or centre through one country of Great Britain to another country of Great Britain

    4. Article 3c. List of approved bodies, institutes or centres in third countries, territories and parts thereof

    5. Article 4. Conditions for the assembly centres for certain consignments of ungulates

    6. Article 5. Protocols for the standardisation of materials and sampling and testing procedures for ungulates

    7. Article 6. Special conditions for certain consignments of ungulates imported into St Pierre and Miquelon and introduced into the Union

    8. Article 7. General conditions for the introduction into Great Britain of certain species of bees

    9. Article 8. General conditions concerning the transport of live animals to Great Britain

    10. Article 9. Time limit for the period of transport to Great Britain of live animals

    11. Article 10. Special conditions regarding the spraying of consignments of live animals transported by air to Great Britain

    12. Article 11. Conditions to be applied following the introduction into Great Britain of certain consignments of ungulates

    13. Article 12. Specific conditions concerning the transit through third countries of certain consignments of ungulates

    14. Article 12a. Derogation for the transit of certain consignments of live bovine animals for breeding and production through Lithuania

    15. Article 13. Conditions to be applied following the introduction into Great Britain of consignments of bees referred to in Article 7

    16. Article 13a. Conditions to be applied following the introduction of consignments of ungulates intended for approved bodies, institutes or centres

  4. CHAPTER III CONDITIONS FOR THE INTRODUCTION OF FRESH MEAT INTO GREAT BRITAIN

    1. Article 14. General conditions for the importation of fresh meat

    2. Article 14b.Supplementary guarantees, fresh meat

    3. Article 15. Conditions to be applied following the importation of unskinned carcases of wild cloven-hoofed game

    4. Article 16. Transit and storage of fresh meat

    5. Article 17. Derogation for transit through Latvia, Lithuania and Poland

    6. Article 17a. Derogation for transit through Croatia of consignments coming from Bosnia and Herzegovina and destined to third countries

  5. CHAPTER IV GENERAL, TRANSITIONAL AND FINAL PROVISIONS

    1. Article 17b.Matters relating to the exercise of powers under this Regulation

    2. Article 18. Certification

    3. Article 19. Transitional provisions

    4. Article 20. Repeal

    5. Article 21. Entry into force

  6. Signature

    1. ANNEX I

      UNGULATES

      1. PART 1

        1. Specific Conditions (see footnotes in each certificate)

      2. PART 2 Models of Veterinary Certificates

      3. PART 3 Addendum for transport of animals by sea

      4. PART 4 Addendum for transport of animals by air

      5. PART 5 Conditions for the approval of assembly centres (referred to in Article 4)

      6. PART 6 Protocols for the standardisation of materials and testing procedures

        1. Tuberculosis (TBL)

        2. Brucellosis ( Brucella abortus ) (BRL)

        3. Brucellosis (Brucella melitensis) (BRL)

        4. Enzootic Bovine Leukosis (EBL)

        5. Bluetongue (BTG)

          1. A. The blocking or competitive ELISA test shall be carried out...

            2. Material and Reagents:

            3. Test format

            4. Test protocol:

            5. Procedure:

            6. Analysis of results:

            7. Preparation of BTV ELISA antigen:

            8. Titration of BTV ELISA antigen:

          2. B. The agar gel immuno-diffusion test shall be carried out according...

            2. Antigen:

            3. Known positive control serum:

            4. Test serum

        6. Epizootic haemorrhagic disease (EHD)

          2. Antigen:

          3. Known positive control serum:

          4. Test serum

        7. Infectious bovine rhinotracheitis (IBR) / infectious pustular vulvo-vaginitis (IPV)

          1. A. The serum neutralisation test shall be carried out according to...

          2. B. Any other test recognised in the framework of Decision 2004/558/EC...

        8. Foot-and-mouth disease (FMD)

          1. A. Collecting oesophageal/pharyngeal samples and testing shall be carried out according...

          2. B. The virus neutralisation test shall be carried out according to...

          3. C. The detection and quantification of antibody by ELISA shall be...

            2. Procedure:

        9. Aujeszky's disease (AJD)

          1. A. The serum neutralisation test shall be carried out according to...

          2. B. Any other test recognised in the framework of Decision 2008/185/EC...

        10. Transmissible gastro-enteritis (TGE)

        11. Swine vesicular disease (SVD)

        12. Classical swine fever (CSF)

        13. Vesicular stomatitis (VS)

      7. PART 7 Import and quarantine animal health conditions for animals imported into St. Pierre and Miquelon within a period of less than six months prior to introduction into the Union

        1. Animal species covered

          2. CHAPTER 1 Residence and quarantine

            1. 1. . . . . . . . . . ....

            2. 2. . . . . . . . . . ....

          3. CHAPTER 2 Animal health tests

            1. 1. . . . . . . . . . ....

            2. 2. . . . . . . . . . ....

              1. 2.1 . . . . . . . . . ....

                1. 2.1.1 . . . . . . . . . ....

                2. 2.1.2 . . . . . . . . . ....

                3. 2.1.3 . . . . . . . . . ....

                4. 2.1.4 . . . . . . . . . ....

                5. 2.1.5 . . . . . . . . . ....

                6. 2.1.6 . . . . . . . . . ....

                7. 2.1.7 . . . . . . . . . ....

                8. 2.1.8 . . . . . . . . . ....

                9. 2.1.9 . . . . . . . . . ....

                10. 2.1.10 . . . . . . . . . ....

                11. 2.1.11 . . . . . . . . . ....

                12. 2.1.12 . . . . . . . . . ....

                13. 2.1.13 . . . . . . . . . ....

    2. ANNEX II

      FRESH MEAT

      1. PART 1

      2. PART 2 Models of veterinary certificates

    3. ANNEX III

    4. ANNEX IV

      ANIMALS REFERRED TO IN ARTICLE 1(1)(b)

      1. PART 1 Lists of third countries, territories or parts thereof

        1. SECTION 1 Parts of third countries or territories referred to in Article 7(2)

      2. PART 2 Tables of animals and the corresponding model veterinary certificates

    5. ANNEX V

      Explanatory notes for completing the veterinary certificates

    6. ANNEX VI

      1. PART 1

      2. PART 2

      3. PART 3 Requirements concerning bodies, institutes or centres in third countries

      4. PART 4 Conditions concerning the approval of bodies, institutes or centres in third countries

        1. 1. Approval must be granted only to those bodies, institutes or...

        2. 2. Where vector protection is required, the approval of a structure...

        3. 3. Each approved body, institute and centre must be assigned an...

        4. 4. Approval must be maintained only as long as the following...

        5. 5. The approval must be withdrawn where the competent authority finds...

        6. 6. Where notification is given of the suspicion of the occurrence...

        7. 7. Where the suspected disease referred to in point 6 is...

        8. 8. Where the approval of a body, institute or centre has...

        9. 9. The competent authority which approved the body, institute or centre...