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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 05/53/EC ,
Reg. (EU) 2018/1262 ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) 2017/1511 ,
Reg. (EU) No 533/2013
Date of approval 01/03/2006 Expiration of approval 31/10/2019
RMS

Co-RMS
BE

DE
Risk Assessment Commission
Category IN, AC Review Report
Remarks Extension of approval period: Reg. (EU) 2017/1511
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, MT, NL, PL, PT, RO, SE, SI, SK, UK
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
Acute Tox. 4 - H302 Acute Tox. 4 - H332
STOT SE 3 - H335 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.05 Dir 05/53  
ARfD 0.2 Dir 05/53  
AOEL 0.06 Dir 05/53  
Other
ARfD 0.05 EMEA 1999 ADI 0,02 JECFA 2004 - ADI: 0.02 ARfD: 0.04 JMPR 2006 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level