Kommisjonens gjennomføringsforordning (EU) 2026/534 av 11. mars 2026 om godkjenning av et preparat av Duddingtonia flagrans NCIMB 30336 som tilsetningsstoff i fôrvarer for beitedyr av storfe, sau og geit, unntatt til melkeproduksjon, og for beitedyr av kamelfamilien, hjortedyr, hester, svin og kaniner (innehaver av godkjenning: International Animal Health Products Pty Ltd, representert i Unionen av SynTech Regulatory Europe GmbH)
Godkjenning av Duddingtonia flagrans som tilsetningsstoff i fôr unntatt beitedyr til melkeproduksjon
Kommisjonsforordning publisert i EU-tidende 12.3.2026
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 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 Duddingtonia flagrans NCIMB 30336. 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 a preparation of Duddingtonia flagrans NCIMB 30336 as a feed additive for all grazing animals, requesting that additive to be classified in the category ‘zootechnical additives’, in the functional group ‘other zootechnical additives’.
(4) Commission Implementing Regulation (EU) 2024/1723 (2) authorised the preparation of Duddingtonia flagrans NCIMB 30336 as a feed additive for grazing animals for milk production of bovine species, sheep, and goats since, due to the lack of data, the European Food Safety Authority (‘the Authority’) could not conclude on the safety of the additive for other grazing animal species and categories in its opinions of 2 July 2020 (3) and 14 November 2023 (4).
(5) Therefore, only the use of that preparation as a feed additive for all grazing animals other than grazing animals for milk production of bovine species, sheep, and goats remains to be addressed in that application.
(6) The Authority concluded in its opinions of 2 July 2020 and 20 March 2025 (5) that, under the proposed conditions of use, the preparation of Duddingtonia flagrans NCIMB 30336 is safe for all grazing bovines, ovines, caprines, rabbits, horses, cervids, camelids and porcine species, as well as for consumers and the environment. The Authority considered that the preparation of Duddingtonia flagrans NCIMB 30336 is not irritant to skin and eyes but is irritant to the respiratory tract and is a respiratory sensitiser, while no conclusion could be drawn on its skin sensitisation potential. The Authority further concluded that the preparation of Duddingtonia flagrans NCIMB 30336 can reduce the number of parasitic nematodes on pasture to the benefit of grazing animals, when used at the recommended application rate of 3 × 104 chlamydospores/kg body weight and per day. It did not consider that there is a need for specific requirements of post-market monitoring. The Authority also verified the report on the methods of analysis of the feed additive in feed submitted by the Reference Laboratory set up by Regulation (EC) No 1831/2003.
(7) On 18 June 2025, the applicant withdrew the application for the authorisation of the preparation for all grazing animals other than bovines, ovines, caprines, camelids, cervids, equines, porcine species and rabbits.
(8) In view of the above, the Commission considers that the preparation of Duddingtonia flagrans NCIMB 30336 satisfies the conditions for authorisation provided for in Article 5 of Regulation (EC) No 1831/2003. Accordingly, the use of that preparation should be authorised for grazing animals of bovine, ovine and caprine species other than for milk production, and for grazing animals of camelid species, cervid species, horses, porcine species and rabbits. Considering the conclusion of the Authority on the safety of the preparation of Duddingtonia flagrans NCIMB 30336 for grazing horses and taking into account that interspecies extrapolation of data can be applied between physiologically similar species (6), the Commission considers that the authorisation of that preparation should be extended to grazing equines. In addition, it is appropriate, for practical and control reasons, to express the dosage of the preparation per kilogram of complete feedingstuff and to provide for the additive to be used only in feed for grazing animals. Finally, the Commission considers that appropriate protective measures should be taken to prevent adverse effects on the health of the users of the additive.
(9) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Plants, Animals, Food and Feed,