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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2008/108 ,
Reg. (EU) No 540/2011
   
Date of approval 01/03/2009 Expiration of approval 28/02/2019
RMS

Co-RMS
UK

FI
Risk Assessment EFSA
Category FU Review Report
Authorisation at national level
Authorised in In progress for
DE, FI
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Fuberidazole
    MRLs Annex II
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Skin Sens. 1 - H317
Carc. 2 - H351 STOT RE 2 - H373
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.0072 Dir 08/108  
ARfD 0.08 Dir 08/108  
AOEL 0.0072 Dir 08/108  
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