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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 540/2011 ,
Reg. (EU) No 810/2011
Old Legislation 2007/21/EC ,
99/01/EC
Date of approval 01/01/2012 Expiration of approval 31/12/2021
RMS

Co-RMS
SE

FR
Risk Assessment EFSA
Category FU Review Report   Confirmatory data 2014
  Renewal 2011
  Inclusion 1998
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, PT, RO, SE, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Kresoxim-methyl (R)
    MRLs Annex II
Classification Reg. 1272/2008
Carc. 2 - H351 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.4 99/1/EC  
ARfD Not applicable 99/1/EC  
AOEL 0.9 99/1/EC  
Other
ARfD unnecessary ADI 0,4 JMPR 2001 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level