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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2008/69/EC ,
2010/39/EU ,
Reg. (EU) No 2017/855 ,
Reg. (EU) No 2018/1796 ,
Reg. (EU) No 540/2011
   
Date of approval 01/01/2009 Expiration of approval 31/12/2019
RMS

Co-RMS
EL

SK
Risk Assessment EFSA
Category IN Review Report   Review report 2017
  Confirmatory data 2010
  Confirmatory data 2013
Remarks The original RMS was Sweden.
Authorisation at national level
Authorised in In progress for
BE, BG, CY, CZ, EL, ES, FR, HR, HU, NL, PL, PT, RO, SK, UK AT
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Diflubenzuron (F) (R)
    MRLs Annex IIIA
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.1 Reg. (EU) 2017/855  
ARfD Not applicable Reg. (EU) 2017/855  
AOEL 0.033 Reg. (EU) 2017/855  
Other
ARfD unnecessary ADI 0,02 JMPR 2002 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level