Contents
THE EUROPEAN COMMISSION,Having regard to the Treaty on the Functioning of the European Union,Having regard to Regulation (EC) No 1069/2009 of the European Parliament and of the Council of 21 October 2009 laying down health rules as regards animal by-products and derived products not intended for human consumption and repealing Regulation (EC) No 1774/2002 (Animal by-products Regulation)note, and in particular the first and third subparagraph of Article 41(3) and point (a) of the first subparagraph of Article 42(2) thereof,Whereas:
(1)The German language version of Commission Regulation (EU) No 142/2011note contains an error in point (1)(b)(i) of Annex XII as regards the requirements for the import and transit of intermediate products destined for the production of medical devices, in vitro diagnostic medical devices and laboratory reagents.
(2)The German language version of Regulation (EU) No 142/2011 should therefore be corrected accordingly. The other language versions are not affected.
(3)The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Plants, Animals, Food and Feed,
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