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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 1031/2013 ,
Reg.(EU) No 2018/185
   
Date of approval 01/02/2014 Expiration of approval 31/01/2024
RMS

Co-RMS
PL

IE
Risk Assessment EFSA
Category FU Review Report   Final Addendum to the Review Reportl 2017
  Review Report 2013
Remarks The original RMS was UK.
Authorisation at national level
Authorised in In progress for
BE, CZ, FI, NL, PL, SK, UK IE
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 0.04 EFSA 2012  
ARfD 0.5 EFSA 2012  
AOEL 0.077 EFSA 2012  
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