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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 22/2013 Old Legislation Dossier complete 2010/244/EU
Date of approval 01/06/2013 Expiration of approval 31/05/2023
RMS

Co-RMS
ES

AT
Risk Assessment EFSA
Category AC Review Report
Remarks The original RMS were Netherlands.
Authorisation at national level
Authorised in In progress for
BE, CY, EL, HR, NL AT, BG, CZ, ES, IT, SI
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Cyflumetofen
    MRLs Annex IIIA
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.17 EFSA 12  
ARfD Not applicable EFSA 12  
AOEL 0.11 EFSA 12  
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