Genetically Modified Organisms

DAS-4Ø278-9

EU register of genetically modified food and feed.

Event DAS-4Ø278-9
Authorisation holder Corteva Agriscience LLC, 9330 Zionsville Road Indianapolis, Indiana 46268-1054, United States, represented in the Union by Corteva Agriscience Belgium BV, Bedrijvenlaan 9, 2800 Mechelen, Belgium
Products (1) Foods and food ingredients containing, consisting of, or produced from DAS-4Ø278-9 maize;
(2) Feed containing, consisting of, or produced from DAS-4Ø278-9 maize;
(3) Products, other than food and feed, containing or consisting of DAS-4Ø278-9 maize for the same uses as any other maize with the exception of cultivation.
Designation DAS-4Ø278-9 maize expresses the AAD-1 protein which confers tolerance to 2,4-dichlorophenoxyacetic acid (2,4-D) and aryloxyphenoxypropionate (AOPP) herbicides.
Labelling (1) For the purposes of the labelling requirements laid down in Articles 13(1) and 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 "maize".

(2) The words "not for cultivation" shall appear on the label of and in documents accompanying products containing or consisting of DAS-4Ø278-9 maize and referred to in Article 2(b) and (c).
Method for detection (1) Event specific real-time quantitative PCR based method for DAS-4Ø278-9 maize; the detection method is validated on the single-trait event using genomic DNA extracted from seeds of DAS-4Ø278-9 maize;
(2) Validated by the EU Reference Laboratory established under Regulation (EC) No 1829/2003, published at
http://gmo-crl.jrc.ec.europa.eu/statusofdossiers.aspx.
Reference material ERM®-BF433 accessible via the Joint Research Centre (JRC) of the European Commission at https://crm.jrc.ec.europa.eu/
Unique identifier DAS-4Ø278-9
Annex II to the Cartagena Protocol http://bch.cbd.int/database/record.shtml?documentid=112239
Conditions or restrictions on the placing on the market Not required
Monitoring plan
Post-market monitoring requirements Monitoring plan for environmental effects conforming with Annex VII to Directive 2001/18/EC.
Date of authorisation 04/07/2017
Legal base Art. 7(3) and Art. 19(3) of the Regulation (EC) No 1829/2003
Commission Implementing Decision (EU) 2017/1212 of 4 July 2017
Amended by Commission Implementing Decision (EU) 2019/239 of 6 February 2019
Amended by Commission Implementing Decision (EU) 2021/1161 of 13 July 2021
Authorisation expiration date 03/07/2027
Further information on risk assessment Opinion of the European Food Safety Authority:
http://registerofquestions.efsa.europa.eu/roqFrontend/questionLoader?question=EFSA-Q-2016-00674
Version: 1.1.3