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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2010/39/EU ,
Reg. (EU) No 540/2011
   
Date of approval 01/01/2009 Expiration of approval 31/12/2018
RMS

Co-RMS
ES

NL
Risk Assessment EFSA
Category AC Review Report   Confirmatory data 2010
  Confirmatory data 2012
Remarks Original inclusion Directive 2008/69/EC The original RMS was the UK.
Authorisation at national level
Authorised in In progress for
BE, BG, CY, EL, ES, HR, IE, IT, LU, NL, PL, PT, RO, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Clofentezine (R)
    MRLs Annex II
  • Annex IIIB
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.02 Dir 08/69  
ARfD Not applicable Dir 08/69  
AOEL 0.01 Dir 08/69  
Other
ADI 0,02 ARfD unnecessary JMPR 2005 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level