L 78/4
ANNEX
Annex XIV to Regulation (EU) No 142/2011 is amended as follows: EN
(1) in Chapter I, Section 1, Table 1 is replaced by the following:
‘Table 1
No
Raw materials (reference to provisions of Regulation (EC) No 1069/2
Import and transit conditions
Third countries’ lists
Certificates/model documents
Processed animal protein, Category 3 materials referred to in (a) The processed animal protein (a) In the case of processed animal proteins (a) In the case of processed an­ including mixtures and Article 10, points (a), (b), (d), (e), must have been produced in ac­ excluding fishmeal: imal protein other than products other than (f), (h), (i), (j), (k), (l) and (m) cordance with Section 1 of Chap­ Third countries listed in Part 1 of Annex those derived from farmed petfood containing such ter II of Annex X; and XIII or Part 1, Section A, of Annex XV to insects: (b) the processed animal protein Annex XV, Chapter 1. protein, and compound Commission Implementing Regulation shall comply with the additional feeds containing such (EU) 2021/404 *, and the following third (b) In the case of processed an­ requirements set out in Section 2 proteins as defined in countries: imal protein derived from of this Chapter.
Article 3(2), point (h), of farmed insects: (AL) Albania Annex XV, Chapter 1a.
Regulation (EC) No 767/2009 (DZ) Algeria (SV) El Salvador.
(b) In the case of fishmeal: Third countries listed in Annex IX to Commission Implementing Regulation (EU) 2021/405 **.
2
Blood products for feed material
8.3.2022
Category 3 materials referred to in The blood products must have been (a) In the case of blood products from un­ Annex XV, Chapter 4(B).
Article 10, point (a) and point (b) produced in accordance with gulates: Third countries or parts of third coun­ (i).
Chapter II, Section 2, of Annex X and Chpater I, Section 5, of Annex XIV tries listed in Part 1 of Annex XIII to Im­ plementing Regulation (EU) 2021/404 or Annex I to Implementing Regulation (EU) 2021/405, from which imports of all categories of fresh meat of the respec­ tive species are authorised.
(b) In the case of blood products from other species: Third countries listed in Part 1 of Annex XIII or Part 1 of Annex XIV to Imple­ menting Regulation (EU) 2021/404.
Official Journal of the European Union
1
Product