Commission Implementing Regulation (EU) No 788/2011
law://eu/reg/2011/788/anx_I@2026-11-13law://eu/reg/2011/788/anx_I@2026-11-13| Common Name, Identification Numbers | IUPAC Name | Puritynote | Date of approval | Expiration of approval | Specific provisions |
|---|---|---|---|---|---|
| Fluazifop-PCAS No 83066-88-0 (fluazifop-P)CIPAC No 467 (fluazifop-P) | (R)-2-{4-[5-(trifluoromethyl)-2-pyridyloxy]phenoxy}propionic acid (fluazifop-P) | ≥ 900 g/kg in fluazifop-P-butylThe following impurity 2-chloro-5-(trifluoromethyl) pyridine must not exceed 1,5 g/kg in the material as manufactured. | 1 January 2012 | 31 December 2021 | PART AOnly uses as herbicide may be authorised.PART BFor the implementation of the uniform principles as referred to in Article 29(6) of Regulation (EC) No 1107/2009, the conclusions of the review report on fluazifop-P, and in particular Appendices I and II thereof, as finalised in the Standing Committee on the Food Chain and Animal Health on 1 February 2013, shall be taken into account.In this overall assessment Member States shall:pay particular attention to consumer safety as regards the occurrence in groundwater of the metabolite compound X;pay particular attention to operator safety and shall ensure that conditions of use include the application of adequate personal protective equipment, where appropriate;pay particular attention to the protection of surface water and groundwater in vulnerable zones;pay particular attention to the risk for non-target plants.Conditions of use shall include risk mitigation measures, where appropriate.The applicant shall submit confirmatory information as regards:(1) the specification of the technical material, as commercially manufactured, including information on the relevance of the impurity R154719;(2) the equivalence between the specifications of the technical material, as commercially manufactured, and the specifications of the test material used in the toxicity studies;(3) the potential long-term risk to herbivorous mammals;(4) the fate and behaviour in the environment of the metabolite compounds X and IV;(5) the potential risk to fish and aquatic invertebrates for the metabolite compound IV.The applicant shall submit to the Commission, the Member States and the Authority the information set out in points (1) and (2) by 30 June 2012 and the information set out in points (3), (4) and (5) by 31 December 2013. |
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