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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 00/67/EC ,
Reg. (EU) 2015/2047 ,
Reg. (EU) No 540/2011
Old Legislation 2010/77/EU ,
Reg. (EU) 2015/1885
Date of approval 01/01/2016 Expiration of approval 31/12/2022
RMS

Co-RMS
AT

PT
Risk Assessment EFSA
Category IN Review Report   List of studies relied upon (AIR 2)
  Renewal of approval 2015
  Inclusion 2005
Remarks The original RMS was UK.
Type Candidate for Substitution (CfS) CfS - criteria two PBT criteria
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, EL, ES, FI, FR, HR, HU, IE, IT, LU, NL, PL, PT, RO, SE, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Fenvalerate (any ratio of constituent isomers (RR, SS, RS & SR) including esfenvalerate) (F) (R)
    MRLs Annex II
Classification Reg. 1272/2008
Acute Tox. 3 - H301 Skin Sens. 1 - H317
Acute Tox. 3 - H331 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.0175 Reg. (EU) 2015/2047  
ARfD 0.0175 Reg. (EU) 2015/2047  
AOEL 0.011 Reg. (EU) 2015/2047  
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