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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 03/31/EC ,
Reg. (EU) No 2018/1262 ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 823/2012
Old Legislation Reg. (EU) 2016/950 ,
Reg. (EU) 2017/1511
Date of approval 01/01/2004 Expiration of approval 31/10/2019
RMS

Co-RMS
DE

HU
Risk Assessment Commission
Category IN Review Report
Remarks Extension of the 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, HU, IT, LT, LV, NL, PL, PT, RO, SE, SI, SK, UK
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. 2 - H330
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: 0.04 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