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Commission Implementing Regulation (EU) 2017/173 of 1 February 2017 amending Regulation (EC) No 1292/2008 and Implementing Regulation (EU) No 887/2011, as regards the name of the holder of the authorisation of Bacillus amyloliquefaciens CECT 5940 and Enterococcus faecium CECT 4515 (Text with EEA relevance. )

Commission Implementing Regulation (EU) 2017/173 of 1 February 2017 amending Regulation (EC) No 1292/2008 and Implementing Regulation (EU) No 887/2011, as regards the name of the holder of the authorisation of Bacillus amyloliquefaciens CECT 5940 and Enterococcus faecium CECT 4515 (Text with EEA relevance. )

Implementing Regulation (EU) 2017/173 · Regulation · 4 articles

Data as of 2026-07-04 · Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗

Amendment to Regulation (EC) No 1292/2008

Article 1

In column 2 of the Annex to Regulation (EC) No 1292/2008 the term ‘Norel SA’ is replaced by the term ‘Evonik Nutrition & Care GmbH’.

Amendment to Implementing Regulation (EU) No 887/2011

Article 2

Implementing Regulation (EU) No 887/2011 is amended as follows: (a) in the title, the term ‘Norel SA’ is replaced by the term ‘Evonik Nutrition & Care GmbH’; (b) in column 2 of the Annex, the term ‘Norel SA’ is replaced by the term ‘Evonik Nutrition & Care GmbH’.

Transitional measures

Article 3

Existing stocks of the additives which are in conformity with the provisions applying before the date of entry into force of this Regulation may continue to be placed on the market and used until they are exhausted.

Entry into force

Article 4

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

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Source: EUR-Lex (Publications Office of the EU), © European Union, reuse permitted under Commission Decision 2011/833/EU.

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