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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2011/47/EU ,
Reg. (EU) No 2018/1266 ,
Reg. (EU) No 540/2011
   
Date of approval 01/06/2011 Expiration of approval 31/05/2024
RMS

Co-RMS
NL

CZ
Risk Assessment EFSA
Category BA Review Report
Remarks Initially non included by Decision 2008/941. Included as from 1 June 2011 following re-submission for inclusion according to Reg. 33/2008.
Authorisation at national level
Authorised in In progress for
NL
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Default MRL of 0.01 mg/kg according to Art 18(1)(b) Reg 396 / 2005.
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI Not applicable 11/47/EU  
ARfD Not applicable 11/47/EU  
AOEL 0,002 11/47/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