MON-877Ø8-9
EU register of genetically modified food and feed.
Event | MON 87708 |
Authorisation holder Name |
Bayer Agriculture BV, Belgium representing Bayer CropScience LP, United States |
Authorisation holder Address |
Bayer Agriculture BV Scheldelaan 460, 2040 Antwerp, Belgium On behalf of Bayer CropScience LP, 800 N. Lindbergh Boulevard, St. Louis, Missouri 63167 – United States. |
Products |
1) Foods and food ingredients containing, consisting of, or produced from MON-877Ø8-9 soybean 2) Feed containing, consisting or produced from MON-877Ø8-9 soybean 3) Products other than food and feed containing or consisting of MON-877Ø8-9 soybean for the same uses as any other soybean with the exception of cultivation |
Designation | The genetically modified soybean MON-877Ø8-9 expresses the DMO (dicamba mono-oxygenase) proteins which confer 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 ’soybean’; 2. The words 'not for cultivation' shall appear on the label of and in the documents accompanying products containing or consisting of MON-877Ø8-9 soybean with the exception of products referred to in point (a) of Article 2; |
Method for detection |
Event specific real-time PCR based method for the quantification of soybean MON-877Ø8-9. Validated on 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 |
AOCS 0311-A and AOCS 0906-A are accessible via the American Oil Chemists Society at http://www.aocs.org/tech/crm. |
Unique identifier | MON-877Ø8-9 |
Annex II to the Cartagena Protocol | https://bch.cbd.int/database/record.shtml?documentid=108079 |
Conditions or restrictions on the placing on the market | Not required |
Monitoring plan | Monitoring plan for environmental effects conforming with Annex VII to Directive 2001/18/EC |
Post-market monitoring requirements | Not required |
Date of authorisation | 24/04/2015 |
Legal base |
Art. 7(3) and 19(3) of the Regulation (EC) No 1829/2003 Commission Decision 2015/700/UE of 24 April 2015 Amended by Commission Implementing Decision (EU) 2019/1579 of 18 September 2019 Amended by Commission Implementing Decision (EU) 2021/184 of 12 February 2021 |
Authorisation expiration date | 26/04/2025 |
Further information on risk assessment | http://www.efsa.europa.eu/en/efsajournal/pub/3355.htm |