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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 890/2014 Old Legislation 2011/253/EU ,
Reg. (EC) No 2076/2002
Date of approval 01/01/2015 Expiration of approval 31/12/2024
RMS FR

Risk Assessment EFSA
Category HB Review Report
Remarks The Co-RMS is Norway
Authorisation at national level
Authorised in In progress for
AT, BE, CY, CZ, DE, EE, EL, FR, HR, HU, IE, IT, LT, LU, MT, NL, PL, PT, RO, SE, SI, UK BG, ES, FI, LV, SK
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 0.008 EFSA 2014  
ARfD 0.3 EFSA 2014  
AOEL 0.016 EFSA 2014  
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