S.L. 437.30 Art. 6(1)(9): (9) (9) must be the animal for human signature of competent the animal human signature of competent Part III - B Veterinary or prescribi treatment Date of last medicinal substances not Annex I, II, Regulation (EEC) [dd/ mm/ (1) (2) Delete what (3) The animal or IV to III - B is optional. (4)

Anémie infectieuse infectious anaemia 7. rabies Rage 8. anthrax Fièvre charbonneuse

SECTION IX

MEDICINAL TREATMENT IDENTIFICATION NUMBER OF ANIMAL .................................................................................

Part I Date and Place of issue of this section: ........................................................................... Competent authority issuing this section of the identification document: ........................ Part II (excludes the animal definitively from slaughter for human consumption, reconfirmed when the animal changes ownership) I, the undersigned owner (2) / representative of the owner (2) declare that described in this identification document is not intended for slaughter consumption (3) Date and Name in capitals and signature of the Name in capitals and Place owner of the animal or his/ her representative of representative authorities

Part III - A (only valid in connection with information in Part III - B) I, the undersigned owner (2) / representative of the owner (2) declare that described in this identification document is intended for slaughter for consumption (4) Date and Name in capitals and signature of the Name in capitals and Place owner of the animal or his/ her representative of representative authorities (informations compulsory for equidae identified in accordance with Part III - A) MEDICATION RECORD surgeon applying and/ Place Substance(s) Name:............. (7) Signature ng medicinal incorporated in - Country Code Address:.......... (7) the medicinal - Postcode product which Postcode:......... (7) treatment with a - Place is/ are not Place:.............. (7) product containing included in included in Tel:................. (8) Annex I, II, III III or IV of or IV of No 2377/ 90 Regulation yyyy] (EEC) No 2377/ 90 (5) (6) Identification number as indicated in Section II (1) of the identification document. is not applicable. may be treated with medicinal products containing substances listed in Annex I, II, III Regulation (EEC) No 2377/ 90 and other substances. Recording of medicinal treatment in Part The animal shall never be slaughtered for human consumption. may be treated with medicinal products containing substances listed in Annex I, II or III

(EEC) No 2377/ 90 and other substances excluding those listed in Annex IV to that animal can only be slaughtered for human consumption after the completion of the withdrawal period of six months following the date of the last treatment, certified obligatory in medicinal products containing substances other than those listed in Annex I, II or III to No 2377/ 90. through published Annexes to Regulation (EEC) No 2377/ 90. information is optional. However, this information may allow the reduction of the withdrawal specified substance is included in Annex I, II or III to Regulation (EEC) No 2377/ 90 after administered. The minimum withdrawal times would then be those established in Article 4 (4) of EEC. address, postcode and place in printed letters. number including country code and regional code. where this Section is issued together with the identification document.