9.—(1) Paragraph (2) applies where, in respect of an equine animal, an issuing body issues—
(a)a duplicate identification document under and in accordance with Article 29, as read with Article 30,
(b)a replacement identification document under and in accordance with Article 32, or
(c)a duplicate identification document or replacement identification document in a case to which Article 17(2) applies.
(2) The issuing body must classify the equine animal as not intended for human consumption by marking accordingly in Part II of Section II (administration of veterinary medicinal products) of that duplicate or replacement identification document (provided a declaration is not already so made in accordance with Article 37(3)).