(fra kommisjonsforordningen)

(1) Regulation (EC) No 1831/2003 provides for the authorisation of additives for use in animal nutrition and for the grounds and procedures for granting and modifying such authorisation.

(2) A preparation of Weizmannia faecalis DSM 32016 was authorised for a period of 10 years as a feed additive for use in feed for suckling and weaned Suidae piglets, poultry for fattening and ornamental birds by Commission Implementing Regulation (EU) 2020/1755 (2) and as a feed additive for use in feed and in water for drinking for all poultry species reared for laying or breeding and for use in water for drinking for all poultry species for fattening, ornamental birds, suckling and weaned Suidae piglets by Commission Implementing Regulation (EU) 2024/1054 (3).

(3) In accordance with Article 13(3) of Regulation (EC) No 1831/2003, an application was submitted on 8 August 2024 for the modification of the terms of the authorisation of the preparation of Weizmannia faecalis DSM 32016 as a feed additive for use in feed and in water for drinking for all poultry species for fattening, reared for breeding and laying and ornamental birds, requesting to allow the simultaneous use of that preparation with the coccidiostat amprolium and a combination of coccidiostats narasin and nicarbazin, which are authorised as feed additives. The request was accompanied by the relevant supporting data.

(4) The European Food Safety Authority (‘the Authority’) concluded in its opinion of 25 June 2025 (4) that the proposed modification in the terms of the authorisation of the preparation of Weizmannia faecalis DSM 32016 would not change the conclusions previously drawn regarding the safety of that additive for the target species, consumers and the environment. The Authority also concluded that the preparation of Weizmannia faecalis DSM 32016 is not a skin or eye irritant but should be considered a skin and respiratory sensitiser, and inhalation and dermal exposure are considered a risk. It also concluded that the use of that preparation is compatible with the coccidiostat amprolium and the combination of coccidiostats narasin and nicarbazin under the currently authorised conditions of use. The Authority did not consider that there is a need for specific requirements for a post-market monitoring.

(5) The Reference Laboratory set up by Regulation (EC) No 1831/2003 considered that the conclusions and recommendations reached in a previous assessment concerning another application for the authorisation of the same additive and verified by the Authority in its opinion of 25 May 2020 (5) are valid and applicable for the current application. In accordance with Article 5(4), point (a), of Commission Regulation (EC) No 378/2005 (6), an evaluation report of the Reference Laboratory was therefore not required.

(6) In view of the above, the Commission considers that the preparation of Weizmannia faecalis DSM 32016 still satisfies the conditions provided for in Article 5 of Regulation (EC) No 1831/2003 when modifying the terms of the authorisation laid down in Implementing Regulations (EU) 2020/1755 and (EU) 2024/1054, by specifying the compatibility of the use of that preparation with the coccidiostat amprolium and a combination of coccidiostats narasin and nicarbazin. In addition, considering that those coccidiostats may not be authorised as feed additives for each of the species or categories listed in Annexes I and II, their simultaneous use with the preparation of Weizmannia faecalis DSM 32016 should only be possible in accordance with their respective conditions of authorisation as feed additives.

(7) Implementing Regulations (EU) 2020/1755 and (EU) 2024/1054 should therefore be amended accordingly.

(8) Since safety reasons do not require the immediate application of the modifications to the conditions of authorisation of the preparation of Weizmannia faecalis DSM 32016 for all poultry species for fattening, reared for breeding and laying and ornamental birds, it is appropriate to provide for a transitional period for interested parties to prepare themselves to meet the new requirements resulting from the modification of the authorisation concerned.

(9) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Plants, Animals, Food and Feed,