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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 05/58/EC ,
Reg. (EU) 2018/917 ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) 2017/841
Date of approval 01/12/2005 Expiration of approval 31/07/2019
RMS

Co-RMS
SE

IT
Risk Assessment Commission
Category AC Review Report   List of studies 2016
  Draft review report
Remarks The original RMS was the Netherlands.
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EL, ES, FI, FR, HU, IE, IT, MT, NL, PL, PT, RO, SE, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Bifenazate (sum of bifenazate plus bifenazate-diazene expressed as bifenazate) (F)
    MRLs Annex II
Classification Reg. 1272/2008
Skin Sens. 1 - H317 STOT RE 2 - H373
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.01 05/58/EC  
ARfD Not applicable 05/58/EC  
AOEL 0.0028 05/58/EC  
Other
ADI: 0.01 ARfD: unnecessary JMPR 2006 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level