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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2008/66 ,
Reg. (EU) No 1124/2013 ,
Reg. (EU) No 540/2011
   
Date of approval 01/01/2009 Expiration of approval 31/12/2018
RMS

Co-RMS
PL

BE
Risk Assessment EFSA
Category HB Review Report   Confirmatory data 2012
  Conditions of approval 2013
Remarks The original RMS was Belgium.
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CZ, DE, EE, ES, FI, FR, HU, IT, LT, LV, NL, PL, RO, SE, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Bifenox (F)
    MRLs Annex IIIA
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.3 Dir 08/66  
ARfD 0.5 Dir 08/66  
AOEL 0.125 Dir 08/66  
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