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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 201/2013 ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 788/2011
Old Legislation 2008/934/EC
Date of approval 01/01/2012 Expiration of approval 31/12/2021
RMS

Co-RMS
FR

IT
Risk Assessment EFSA
Category HB Review Report   Confirmatory data 2015
  Approval 2011
  Conditions of approval 2013
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, MT, NL, PL, PT, RO, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Fluazifop-P (sum of all the constituent isomers of fluazifop, its esters and its conjugates, expressed as fluazifop)
    MRLs Annex II
Classification Reg. 1272/2008
Repr. 2 - H361d Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.01 EFSA 10  
ARfD 0.017 EFSA 10  
AOEL 0.02 EFSA 10  
Other
 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level