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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
    Old Legislation 06/133/EC ,
Reg. (EU) No 540/2011
Date of approval 01/01/2007 Expiration of approval 12/04/2013
RMS IE

Risk Assessment Commission
Category FU Review Report
Remarks Part of Dir 06/133 suspended by Court of First Instance (19/7/07) until final judgment that was delivered on 12 April 2013 dismissing the action against the Commission.
Authorisation at national level
No authorisation in place
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Flusilazole (F) (R)
    MRLs Annex V
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Carc. 2 - H351
Repr. 1B - H360D Aquatic Chronic 2 - H411
Toxicological information
Reference values Source Remark
ADI 0.002 Dir 06/133  
ARfD 0.005 Dir 06/133  
AOEL 0.005 Dir 06/133  
Other
ADI 0,007 ARfD 0,02 JMPR 2007 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level