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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2011/48/EU ,
Reg. (EU) No 540/2011
   
Date of approval 01/06/2011 Expiration of approval 31/05/2021
RMS

Co-RMS
IT

RO
Risk Assessment EFSA
Category RO 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.
Type Candidate for Substitution (CfS) CfS - criteria low ADI / ARfD / AOEL
Authorisation at national level
Authorised in In progress for
FR, NL, RO IT
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
Acute Tox. 1 - H300 Acute Tox. 1 - H310
Acute Tox. 1 - H330 Repr. 1B - H360D
STOT RE 1 - H372 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI Not applicable 11/48/EU  
ARfD Not applicable 11/48/EU  
AOEL 0,0012 x 10<sup>-3</sup> 11/48/EU  
Other
AOEL Acute: 0,0023 x 10<sup>-3</sup>  
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level