Genetically Modified Organisms

MON-941ØØ-2

EU register of genetically modified food and feed.

Event MON 94100
Authorisation holder Name Bayer CropScience LP
Authorisation holder Address 800 N. Lindbergh Boulevard,
St. Louis, Missouri 63167, United States of America

Represented in the Union by: Bayer Agriculture BV, Scheldelaan 460, 2040 Antwerp, Belgium.
Products 1.) foods and food ingredients containing, consisting of or produced from genetically modified oilseed rape MON941ØØ-2

2.) feed containing, consisting of or produced from genetically modified oilseed rape MON-941ØØ-2

3.) products containing or consisting of genetically modified oilseed rape MON-941ØØ-2 for uses other than those provided for in points (1) and (2), with the exception of cultivation.
Designation The genetically modified oilseed rape MON-941ØØ-2 expresses the dmo gene, which confers tolerance to dicamba-based herbicides
Labelling (1) For the purposes of the specific labelling requirements laid down in Article 13(1) and Article 25(2) of Regulation (EC) No 1829/2003, and in Article 4(6) of Regulation (EC) No 1830/2003, the ’name of the organism’ shall be ’oilseed rape’;

(2) The words 'not for cultivation' shall appear on the label of and in documents accompanying products containing or consisting of genetically modified oilseed rape MON941ØØ-2 with the exception of products referred to in point (a) of Article 2.
Method for detection Event specific real-time quantitative PCR based method for the detection of genetically modified oilseed rape MON941ØØ-2

Validated by the EU Reference Laboratory established under Regulation (EC) No 1829/2003, published at:
URL: http://gmo-crl.jrc.ec.europa.eu/StatusOfDossiers.aspx
Reference material Reference Material: AOCS 0421-A is accessible via the American Oil Chemists Society at https://www.aocs.org/crm
Unique identifier MON941ØØ-2
Annex II to the Cartagena Protocol BCH-DEC-EU-265494-1
Conditions or restrictions on the placing on the market Not applicable
Monitoring plan Monitoring plan for environmental effects conforming with Annex VII to Directive 2001/18/EC
Post-market monitoring requirements Not appropriate
Date of authorisation 24/02/2023
Legal base Commission Implementing Decision (EU) 2023/416 of 22 February 2023
Authorisation expiration date 23/02/2033
Further information on risk assessment Opinion of the European Food Safety Authority:
https://www.efsa.europa.eu/en/efsajournal/pub/7411
Version: 1.1.3