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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 2019/716 ,
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.
Reg. (EU) No 2019/716 amended the Conditions of Approval:
Plant protection products containing cyflumetofen shall only be authorised for uses where the level of metabolite B3 in groundwater is expected to be below 0,1 μg/L.
Withdrawal authorisations by 30 November 2019.
Max period of grace: 30 May 2020
Authorisation at national level
Authorised in In progress for
BE, BG, CY, EL, ES, HR, IT, NL, PT AT, CZ, SI, UK
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