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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 02/37/EC ,
Reg. (EU) 2016/1426 ,
Reg. (EU) 2016/950 ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 823/2012
   
Date of approval 01/11/2016 Expiration of approval 31/10/2031
RMS

Co-RMS
AT

DK
Risk Assessment EFSA
Category HB Review Report   Renewal 2016
  List of studies relied upon (AIR 3)
  Inclusion 2002
Remarks The original RMS was Sweden.

Extension of the approval period (Reg. (EU) 2016/950).
Authorisation at national level
Authorised in In progress for
AT, BE, CZ, DE, DK, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, PT, RO, SE, SI, SK, UK BG
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Ethofumesate (Sum of ethofumesate, 2-keto–ethofumesate, open-ring-2-keto-ethofumesate and its conjugate, expressed as ethofumesate)
    MRLs Annex II
Classification Reg. 1272/2008
Aquatic Chronic 2 - H411
Toxicological information
Reference values Source Remark
ADI 1.0 Reg. (EU) 2016/1426  
ARfD Not applicable Dir 02/37, Reg. (EU) 2016/1426  
AOEL 2.5 Dir 02/37, Reg. (EU) 2016/1426  
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