Kommisjonens gjennomføringsforordning (EU) 2026/103 av 15. januar 2026 om fornyet godkjenning av et preparat av Enterococcus lactis DSM 7134 som tilsetningsstoff i fôr til purker (innehaver av godkjenningen: Lactosan GmbH&Co.KG) og oppheving av gjennomføringsforordning (EU) nr. 1083/2014
Fornyet godkjenning av av et preparat av Enterococcus lactis DSM 7134 som tilsetningsstoff i fôr til purker
Kommisjonsforordning publisert i EU-tidende 16.1.2026
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 and renewing such an authorisation.
(2) A preparation of Enterococcus lactis (originally assigned to the Enterococcus faecium species) DSM 7134, was authorised for a period of 10 years as a feed additive for sows by Commission Implementing Regulation (EU) No 1083/2014 (2).
(3) In accordance with Article 14(1) of Regulation (EC) No 1831/2003, an application was submitted for the renewal of the authorisation of the preparation of Enterococcus lactis DSM 7134 as a feed additive for sows, requesting the additive to be classified in the additive category ‘zootechnical additives’ and in the functional group ‘gut flora stabilisers’. That application was accompanied by the particulars and documents required under Article 14(2) of Regulation (EC) No 1831/2003.
(4) The European Food Safety Authority (‘the Authority’) concluded in its opinion of 19 March 2025 (3) that the preparation of Enterococcus lactis DSM 7134 remains safe for sows, as well as for the consumers and the environment under the conditions of use currently authorised. It also concluded that the preparation of Enterococcus lactis DSM 7134 in its powder form is not irritant to skin and eyes but no such conclusion is possible for the granulated form of the additive. Both forms of the additive should be considered skin and respiratory sensitisers and any exposure through skin and respiratory tract is considered a risk. The Authority also indicated that there is no need for assessing the efficacy of the preparation of Enterococcus lactis DSM 7134, as the application for renewal of the authorisation does not include a proposal for amending or supplementing the conditions of the original authorisations which would have an impact on the efficacy of the additive. The Authority did not consider that there is a need for specific requirements of post-market monitoring.
(5) The Reference Laboratory set up by Regulation (EC) No 1831/2003 considered that the conclusions and recommendations reached in the assessment carried out regarding the method of analysis of the preparation of Enterococcus lactis DSM 7134 as a feed additive in the context of the previous authorisation are valid and applicable for the current application. In accordance with Article 5(4), point (c), of Commission Regulation (EC) No 378/2005 (4), an evaluation report of the Reference Laboratory is therefore not required.
(6) In view of the above, the Commission considers that the preparation of Enterococcus lactis DSM 7134 satisfies the conditions provided for in Article 5 of Regulation (EC) No 1831/2003. Accordingly, the authorisation of that additive should be renewed. 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. Those protective measures should be without prejudice to other workers’ safety requirements under Union law.
(7) As a consequence of the renewal of the authorisation of the preparation of Enterococcus lactis DSM 7134 as a feed additive, Implementing Regulation (EU) No 1083/2014 should be repealed.
(8) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Plants, Animals, Food and Feed,