The certificate accompanying medicated feedingstuffs manufactured in another Member State of the European Union or party to the Agreement on the European Economic Area when they are imported corresponds to a model laid down by decision of the Director General of the Agence nationale de sécurité sanitaire de l’alimentation, de l’environnement et du travail and which states:
1° The name or business name and address of the approved manufacturer and, if separate, those of the distributor ;
2° The name of the medicated feed;
3° The type of animal for which the medicated feed is intended;
4° The name, qualitative and quantitative composition and marketing authorisation number of the medicated premix used to manufacture the medicated feed;
5° The name and marketing authorisation number of the medicated premix authorised in France with a similar qualitative and quantitative composition;
6° The rate of incorporation of the premix;
7° The quantity of medicated feed;
8° The name and address of the recipient.