Kommisjonens gjennomføringsforordning (EU) 2025/277 av 12. februar 2025 om godkjenning av preparat av Loigolactobacillus coryniformis DSM 34345 som et tilsetningsstoff i fôr til alle dyrearter
Godkjenning av Loigolactobacillus coryniformis DSM 34345 som tilsetningsstoff i fôr til alle dyrearter
Kommisjonsforordning publisert i EU-tidende 13.2.2025
Bakgrunn
(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 such an authorisation.
(2) In accordance with Article 7 of Regulation (EC) No 1831/2003, an application was submitted for the authorisation of a preparation of Loigolactobacillus coryniformis DSM 34345. That application was accompanied by the particulars and documents required under Article 7(3) of Regulation (EC) No 1831/2003.
(3) The application concerns the authorisation of the preparation of Loigolactobacillus coryniformis DSM 34345 as a feed additive for all animal species, requesting that additive to be classified in the category ‘technological additives’ and in the functional group ‘silage additives’.
(4) The European Food Safety Authority (‘the Authority’) in its opinion of 26 June 2024 (2) concluded that Loigolactobacillus coryniformis DSM 34345 and the formulated additive are safe for all animal species, consumers and the environment. Regarding user safety, the Authority concluded that the additive should be considered as a potential skin and respiratory sensitiser, that any exposure through skin and respiratory tract is considered a risk and that one preparation was shown not to be irritant to skin or eyes. It further concluded that the addition of Loigolactobacillus coryniformis DSM 34345 at a minimum level of 1 × 108 CFU/kg fresh plant material has the potential to improve the production of silages from all fresh plant materials by enhancing the preservation of nutrients. The Authority also verified the report on the method of analysis of the feed additive in feed submitted by the Reference Laboratory set up by Regulation (EC) No 1831/2003.
(5) In view of the above, the Commission considers that the preparation of Loigolactobacillus coryniformis DSM 34345 satisfies the conditions provided for in Article 5 of Regulation (EC) No 1831/2003. Accordingly, the use of that preparation should be authorised. In addition, the Commission considers that appropriate protective measures should be taken to prevent adverse effects on the health of the users of the additive.
(6) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Plants, Animals, Food and Feed,