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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2011/23/EU ,
Reg. (EU) No 540/2011
   
Date of approval 01/04/2011 Expiration of approval 31/03/2021
RMS

Co-RMS
IT

HU
Risk Assessment EFSA
Category IN Review Report
Remarks Initially non included by Decision 2009/241. Included as from 1 April 2011 following re-submission for inclusion according to Reg. 33/2008
Authorisation at national level
Authorised in In progress for
ES, HU, IT, PT
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Triflumuron (F)
    MRLs Annex II
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.014 EFSA 11  
ARfD Not applicable EFSA 11  
AOEL 0.036 EFSA 11  
Other
ARfD of metabolite  
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level