Commission Implementing Regulation (EU) 2020/377

law://eu/reg/2020/377@2026-11-13

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THE EUROPEAN COMMISSION,Having regard to the Treaty on the Functioning of the European Union,Having regard to Regulation (EC) No 1831/2003 of the European Parliament and of the Council of 22 September 2003 on additives for use in animal nutrition^note, and in particular Article 9(2) thereof,Whereas:

(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 authorisation.

(2)In accordance with Article 7 of Regulation (EC) No 1831/2003 an application was submitted for the authorisation of sodium selenate as a feed additive for ruminants.

(3)The applicant requested sodium selenate to be classified in the additive category ‘nutritional additives’. The application was accompanied by the particulars and documents required under Article 7(3) of Regulation (EC) No 1831/2003.

(4)The European Food Safety Authority (‘the Authority’) concluded in its opinion of 3 July 2019^note that, under the proposed conditions of use, sodium selenate does not have adverse effects on animal health, consumer safety or the environment. It also concluded that the additive is considered a skin and eye irritant and a skin and respiratory sensitiser. Therefore, the Commission considers that appropriate protective measures should be taken to prevent adverse effects on human health, in particular as regards the users of the additive. The Authority also concluded that the additive is an efficacious source of selenium for ruminants. The Authority does not consider that there is a need for specific requirements of post-market monitoring. It also verified the reports on the method of analysis of the feed additives in feed submitted by the Reference Laboratory set up by Article 21 of Regulation (EC) No 1831/2003.

(5)The assessment of sodium selenate shows that the conditions for authorisation, as provided for in Article 5 of Regulation (EC) No 1831/2003, are satisfied. Accordingly, the use of this additive should be authorised as specified in the Annex to this Regulation.

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

HAS ADOPTED THIS REGULATION:

Article 1 #

The substance specified in the Annex, belonging to the additive category ‘nutritional additives’ and to the functional group ‘compounds of trace elements’, is authorised as an additive in animal nutrition, subject to the conditions laid down in that Annex.

Article 2 #

This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union.

Identification number of the additive	Additive	Composition, chemical formula, description, analytical method.	Species or category of animal	Maximum age	Maximum content	Other provisions	End of period of authorisation
Selenium in mg/kg of complete feed with a moisture content of 12 %
Category of nutritional additives. Functional group: compounds of trace elements
3b803	Sodium selenate	Characterisation of the additiveSodium selenate, as a powder, with a minimum content of 41 % seleniumCharacterisation of the active substanceDisodium selenateChemical formula: Na₂SeO₄CAS number 13410-01-0Analytical method^noteFor the quantification of total selenium in the feed additive:TitrationFor the quantification of total sodium in sodium selenate:Atomic Absorption Spectrometry (AAS) – EN ISO 6869:2000; orInductively Coupled Plasma Atomic Emission Spectrometry (ICP-AES) – EN 15510:2007For the quantification of total selenium in premixtures, feed materials and compound feed:Hydride Generation Atomic Absorption Spectrometry (HGAAS) after microwave digestion – EN 16159:2012	Ruminants	—	0,50 (total)	1. Sodium selenate may be placed on the market and used as an additive consisting of a preparation.2. The additive shall be incorporated into feed in the form of a premixture.3. For users of the additive and premixture, feed business operators shall establish operational procedures and organisational measures to address potential risks by inhalation, dermal contact or eye contact. Where those risks cannot be eliminated or reduced to a minimum by such procedures and measures, the additive and premixture shall be used with appropriate personal protective equipment.	26 March 2030

Commission Implementing Regulation (EU) 2020/377

Commission Implementing Regulation (EU) 2020/377

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