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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 07/25/EC ,
Reg. (EU) 2018/917 ,
Reg. (EU) No 540/2011
   
Date of approval 01/10/2007 Expiration of approval 31/07/2019
RMS

Co-RMS
IT

BG
Risk Assessment EFSA
Category IN, AC Review Report   Confirmatory data 2014
  Inclusion 2006
Remarks The original RMS was the UK.
Type Candidate for Substitution (CfS) CfS - criteria low ADI / ARfD / AOEL
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, EE, EL, ES, FI, HR, HU, IE, IT, LU, MT, NL, PL, PT, RO, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Dimethoate
    MRLs Annex II
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Acute Tox. 4 - H312
Toxicological information
Reference values Source Remark
ADI 0.001 EFSA 2013  
ARfD 0.01 EFSA 2013  
AOEL 0,001 EFSA 2013  
Other
ARfD 0,02 - ADI 0,002 JMPR 2003 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level