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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2009/37 ,
Reg. (EU) No 540/2011
   
Date of approval 01/12/2009 Expiration of approval 30/11/2021
RMS

Co-RMS
AT

DE
Risk Assessment EFSA
Category IN Review Report   Specification 2010
  Confirmatory data 2012
Remarks Extension of the approval period: Reg. (EU) 2017/555
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, EL, FR, HU, IT, LT, LU, LV, PL, PT, RO, SK, UK EE
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Cypermethrin (cypermethrin including other mixtures of constituent isomers (sum of isomers)) (F)
    MRLs Annex II
  • Annex IIIB
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.04 EFSA 08  
ARfD 0.125 EFSA 08  
AOEL 0.02 EFSA 08  
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