PLANTS

Language selector

Accessibility tools

Navigation path

Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2010/27/EU ,
Reg. (EU) No 540/2011
   
Date of approval 01/07/2010 Expiration of approval 30/06/2020
RMS

Co-RMS
NL

BE
Risk Assessment EFSA
Category FU Review Report
Remarks Initially non included by Decision 2008/748. Included as from 1 July 2010 following re-submission for inclusion according to Reg. 33/2008.
Authorisation at national level
Authorised in In progress for
BE, NL
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Triflumizole: Triflumizole and metabolite FM-6-1(N-(4-chloro-2-trifluoromethylphenyl)-n-propoxyacetamidine), expressed as Triflumizole (F)
    MRLs Annex II
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Skin Sens. 1 - H317
Repr. 1B - H360D STOT RE 2 - H373
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.05 2010/27/EU  
ARfD 0.1 2010/27/EU  
AOEL 0.05 2010/27/EU  
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