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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2009/154/EC ,
Reg. (EU) 2017/1527 ,
Reg. (EU) No 540/2011
   
Date of approval 01/04/2010 Expiration of approval 31/03/2023
RMS

Co-RMS
DE

AT
Risk Assessment EFSA
Category FU Review Report
Remarks Extension of approval period: Reg. (EU) 2017/1527
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, EE, EL, ES, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, PT, RO, SE, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Cyflufenamid: sum of cyflufenamid (Z-isomer) and its E-isomer
    MRLs Annex IIIA
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.04 09/154/EC  
ARfD 0.05 09/154/EC  
AOEL 0.03 09/154/EC  
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