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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 460/2014 Old Legislation 03/31/EC ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 823/2012
Date of approval 01/01/2004 Expiration of approval 30/04/2014
RMS DE

Risk Assessment Commission
Category IN, AC Review Report
Authorisation at national level
Authorised in In progress for
PT
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Cyfluthrin (cyfluthrin including other mixtures of constituent isomers (sum of isomers)) (F)
    MRLs Annex II
  • Annex IIIB
Classification Reg. 1272/2008
Acute Tox. 2 - H300 Acute Tox. 3 - H331
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.003 Dir 03/31  
ARfD 0.02 Dir 03/31  
AOEL 0.02 Dir 03/31  
Other
ADI 0.02 JECFA&ECCO 1997ADI 0,003 EMEA 2001 - ADI: 0.04 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