Commission Implementing Decision of 6 November 2013 authorising the placing on the market of pollen produced from maize MON 810 (MON-ØØ81Ø-6) pursuant to Regulation (EC) No 1829/2003 of the European Parliament and of the Council (notified under document C(2013) 4743) (Only the Dutch and French texts are authentic) (Text with EEA relevance) (2013/649/EU) (revoked)
EU Decision 2013/649 · Adopted 6 November 2013 · Extends to United Kingdom
Commission Implementing Decision
of 6 November 2013
authorising the placing on the market of pollen produced from maize MON 810 (MON-ØØ81Ø-6) pursuant to Regulation (EC) No 1829/2003 of the European Parliament and of the Council
(notified under document C(2013) 4743)
(Only the Dutch and French texts are authentic)
(Text with EEA relevance)
(2013/649/EU) (revoked)
F1. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Annotations to the whole text
Textual amendments
- F1
Decision revoked (E.W.S.) (1.4.2025) by The Food and Feed (Regulated Products) (Amendment, Revocation, Consequential and Transitional Provision) Regulations 2025 (S.I. 2025/361), reg. 1(2), Sch. 6 para. 19 (with reg. 23)
Contents
- 1Genetically modified organism and unique identifier Repealed
- 2Authorisation Repealed
- 3Labelling Repealed
- 4Register Repealed
- 5Authorisation holder Repealed
- 6Validity Repealed
- 7Addressee Repealed
- Annex Repealed
- (a)Applicant and Authorisation holder Repealed
- (b)Designation and specification of the products Repealed
- (c)Labelling Repealed
- (d)Method for detection Repealed
- (e)Unique identifier Repealed
- (f)Information required under Annex II to the Cartagena Protocol on Biosafety to the Convention on Biological Diversity Repealed
- (g)Conditions or restrictions on the placing on the market, use or handling of the products Repealed
- (h)Monitoring plan Repealed
- (i)Post market monitoring requirements for the use of the food for human consumption Repealed
- Repealed
1Genetically modified organism and unique identifierF1
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2AuthorisationF1
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3LabellingF1
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4RegisterF1
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5Authorisation holderF1
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6ValidityF1
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7AddresseeF1
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(a)Applicant and Authorisation holderF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(b)Designation and specification of the productsF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(c)LabellingF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(d)Method for detectionF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(e)Unique identifierF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(f)Information required under Annex II to the Cartagena Protocol on Biosafety to the Convention on Biological DiversityF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(g)Conditions or restrictions on the placing on the market, use or handling of the productsF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(h)Monitoring planF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(i)Post market monitoring requirements for the use of the food for human consumptionF1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .