Commission Implementing Regulation (EU) 2015/2307 of 10 December 2015 concerning the authorisation of menadione sodium bisulphite and menadione nicotinamide bisulphite as feed additives for all animal species (Text with EEA relevance)

Type Implementing Regulation
Publication 2015-12-11
State In force
Text As published
Department European Commission
Source EUR-Lex
articles 3

This is the act as published. Later amendments are not folded into the text below: each one is a separate act in this repository and an entry in this law's history.

Reform history JSON API
11.12.2015 EN Official Journal of the European Union L 326/49

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 1, and in particular Article 9(2) thereof,

Whereas:

HAS ADOPTED THIS REGULATION:

Article 1

Authorisation

The substances specified in the Annex, belonging to the additive category ‘nutritional additives’ and to the functional group ‘vitamins, pro-vitamins and chemically well-defined substances having similar effect’, are authorised as feed additives in animal nutrition subject to the conditions laid down in that Annex.

Article 2

Transitional measures

1.

The substances specified in the Annex and premixtures containing these substances, which are produced and labelled before 30 June 2016 in accordance with the rules applicable before 31 December 2015 may continue to be placed on the market and used until the existing stocks are exhausted.

2.

Compound feed and feed materials containing the substances specified in the Annex which are produced and labelled before 31 December 2016 in accordance with the rules applicable before 31 December 2015 may continue to be placed on the market and used until the existing stocks are exhausted if they are intended for food-producing animals.

3.

Compound feed and feed materials containing the substances specified in the Annex which are produced and labelled before 31 December 2017 in accordance with the rules applicable before 31 December 2015 may continue to be placed on the market and used until the existing stocks are exhausted if they are intended for non-food-producing animals.

Article 3

Entry into force

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

This Regulation shall be binding in its entirety and directly applicable in all Member States.

Done at Brussels, 10 December 2015.

For the Commission

The President

Jean-Claude JUNCKER

2

Council Directive 70/524/EEC of 23 November 1970 concerning additives in feedingstuffs (OJ L 270, 14.12.1970, p. 1).

3

EFSA Journal 2014;12(1):3532.

ANNEX

Identification number of the additive Name of the holder of authorisation Additive Composition, chemical formula, description, analytical method Species or category of animal Maximum age Minimum content Maximum content Other provisions End of period of authorisation
Identification number of the additive Name of the holder of authorisation Additive Composition, chemical formula, description, analytical method Species or category of animal Maximum age mg of active substance/kg of complete feedingstuff with a moisture content of 12 % mg of active substance/kg of complete feedingstuff with a moisture content of 12 % Other provisions End of period of authorisation
Category of nutritional additives. Functional group: vitamins, pro-vitamins and chemically well-defined substances having similar effect Category of nutritional additives. Functional group: vitamins, pro-vitamins and chemically well-defined substances having similar effect Category of nutritional additives. Functional group: vitamins, pro-vitamins and chemically well-defined substances having similar effect Category of nutritional additives. Functional group: vitamins, pro-vitamins and chemically well-defined substances having similar effect Category of nutritional additives. Functional group: vitamins, pro-vitamins and chemically well-defined substances having similar effect Category of nutritional additives. Functional group: vitamins, pro-vitamins and chemically well-defined substances having similar effect Category of nutritional additives. Functional group: vitamins, pro-vitamins and chemically well-defined substances having similar effect Category of nutritional additives. Functional group: vitamins, pro-vitamins and chemically well-defined substances having similar effect Category of nutritional additives. Functional group: vitamins, pro-vitamins and chemically well-defined substances having similar effect Category of nutritional additives. Functional group: vitamins, pro-vitamins and chemically well-defined substances having similar effect
3a710 — ‘Menadione sodium bisulphite’ or ‘Vitamin K3’ Additive composition Menadione sodium bisulphite Chromium ≤ 45 mg/kg Characterisation of the active substance Menadione sodium bisulphite C11H9NaO5S·3H2O CAS No: 6147-37-1 Produced by chemical synthesis Purity: min. 96 % MSB complex which corresponds to min. 50 % menadione. Method of Analysis 4 — For the determination of menadione sodium bisulphite in the feed additive: a spectrophotometric method using a visible detector at 635 nm (VDLUFA -Bd.III 13.7.1). — For the determination of menadione sodium bisulphite in premixtures and feedingstuffs: Normal Phase High-Performance Liquid Chromatograph coupled to UV detector-decree 29/04/2010, Official Italian Journal No 120 25/5/2010. All animal species — — — 1. The additive shall be incorporated into feed in the form of a premixture. 2. In the directions for use of the additive and premixtures, indicate the storage and stability conditions. 3. The following equivalency shall be used if the amount of the additive is labelled: 1 mg vitamin K3 = 1 mg of menadione = 2 mg of menadione sodium bisulphite. 4. Appropriate measures shall be taken to avoid the chromium emission in the air and prevent the exposure by inhalation or by dermal route. If such measures are technically not feasible or not sufficient, protective measures shall be taken according to national regulations implementing Union legislation on health and safety at work including Council Directives 89/391/EEC5, 89/656/EEC6, 92/85/EEC7 and 98/24/EC8 and Directive 2004/37/EC of the European Parliament and of the Council9. 5. Appropriate protective gloves, respiratory and eye protection according to Council Directive 89/686/EEC10 shall be worn during handling. 31 December 2025
3a711 — ‘Menadione nicotinamide bisulphite’ or ‘Vitamin K3’ Additive composition Menadione nicotinamide bisulphite Chromium ≤ 142 mg/kg Characterisation of the active substance Menadione nicotinamide bisulphite C11H9O5S·C6H7N2O CAS No: 73581-79-0 Produced by chemical synthesis Purity: min. 96 % menadione nicotinamide bisulphite complex which corresponds to min. 43,9 % menadione and min. 31,2 % nicotinamide Method of Analysis 4 — For the determination menadione nicotinamide bisulphite in the feed additive: a spectrophotometric method using a visible detector at 635 nm (VDLUFA — Bd.III 13.7.1). — For the determination of menadione nicotinamide bisulphite in premixtures and feedingstuffs: Normal Phase High-Performance Liquid Chromatograph-decree 29/04/2010, Official Italian Journal No 120 25/5/2010. All animal species — — — 1. The additive shall be incorporated into feed in the form of a premixture. 2. In the directions for use of the additive and premixtures, indicate the storage and stability conditions. 3. The following equivalency shall be used if the amount of the additive is labelled: 1 mg vitamin K3 = 1 mg of menadione = 2,27 mg of menadione nicotinamide bisulphite. 4. Appropriate measures shall be taken to avoid the chromium emission in the air and prevent the exposure by inhalation or by dermal route. If such measures are technically not feasible or not sufficient, protective measures shall be taken according to national regulations implementing Union legislation on health and safety at work including Directives 89/391/EEC, 89/656/EEC, 92/85/EEC, 98/24/EC and 2004/37/EC. 5. Appropriate protective gloves, respiratory and eye protection according to Directive 89/686/EEC shall be worn during handling. 31 December 2025
4

Details of the analytical methods are available at the following address of the European Union Reference Laboratory for Feed Additives: https://ec.europa.eu/jrc/en/eurl/feed-additives/evaluation-reports

5

Council Directive 89/391/EEC of 12 June 1989 on the introduction of measures to encourage improvements in the safety and health of workers at work (OJ L 183, 29.6.1989, p. 1).

6

Council Directive 89/656/EEC of 30 November 1989 on the minimum health and safety requirements for the use by workers of personal protective equipment at the workplace (OJ L 393, 30.12.1989, p. 18).

7

Council Directive 92/85/EEC of 19 October 1992 on the introduction of measures to encourage improvements in the safety and health at work of pregnant workers and workers who have recently given birth or are breastfeeding (OJ L 348, 28.11.1992, p. 1).

8

Council Directive 98/24/EC of 7 April 1998 on the protection of the health and safety of workers from the risks related to chemical agents at work (OJ L 131, 5.5.1998, p. 11).

9

Directive 2004/37/EC of the European Parliament and of the Council of 29 April 2004 on the protection of workers from the risks related to exposure to carcinogens or mutagens at work (OJ L 158, 30.4.2004, p. 50).

10

Council Directive 89/686/EEC of 21 December 1989 on the approximation of the laws of the Member States relating to personal protective equipment (OJ L 399, 30.12.1989, p. 18).

Reading this document does not replace reading the official text published in the Official Journal of the European Union. We assume no responsibility for any inaccuracies arising from the conversion of the original to this format.

This text is published under EUR-Lex's own terms of reuse, not a Legalize or public-domain licence. EUR-Lex
Creative Commons Attribution 4.0 International (CC BY 4.0)
© European Union, https://eur-lex.europa.eu — Source: EUR-Lex (Publications Office of the European Union). Reused under the Creative Commons Attribution 4.0 International (CC BY 4.0) licence. Only EU legislation published in the printed Official Journal of the European Union is deemed authentic; consolidated texts are reproduced here for documentation purposes and have been reformatted to Markdown.