Commission Regulation (EU) 2021/1973 of 12 November 2021 correcting the German language version of Regulation (EU) No 142/2011 implementing Regulation (EC) No 1069/2009 of the European Parliament and of the Council laying down health rules as regards animal by-products and derived products not intended for human consumption and implementing Council Directive 97/78/EC as regards certain samples and items exempt from veterinary checks at the border under that Directive (Text with EEA relevance)
Date: 2021-11-12
Institutions: Directorate-General for Translation, European Commission
Subjects: animal health, animal product, by-product, customs regulations, health control, health risk, import (EU), veterinary inspection, waste management








L_2021402EN.01000401.xml










15.11.2021   


EN


Official Journal of the European Union


L 402/4








            COMMISSION REGULATION (EU) 2021/1973
of 12 November 2021
         
correcting the German language version of Regulation (EU) No 142/2011 implementing Regulation (EC) No 1069/2009 of the European Parliament and of the Council laying down health rules as regards animal by-products and derived products not intended for human consumption and implementing Council Directive 97/78/EC as regards certain samples and items exempt from veterinary checks at the border under that Directive
(Text with EEA relevance)


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) (1), 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 142/2011 (2) 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,





HAS ADOPTED THIS REGULATION:



Article 1

(does not concern the English language)



Article 2
This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union.




This Regulation shall be binding in its entirety and directly applicable in all Member States.
Done at Brussels, 12 November 2021.


For the Commission


The President

Ursula VON DER LEYEN
            





(1)  
            OJ L 300, 14.11.2009, p. 1.

(2)  Commission Regulation (EU) No 142/2011 of 25 February 2011 implementing Regulation (EC) No 1069/2009 of the European Parliament and of the Council laying down health rules as regards animal by-products and derived products not intended for human consumption and implementing Council Directive 97/78/EC as regards certain samples and items exempt from veterinary checks at the border under that Directive (OJ L 54, 26.2.2011, p. 1).