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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 06/39/EC ,
Reg. (EU) No 2018/524 ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) No 487/2014
Date of approval 01/02/2007 Expiration of approval 30/04/2019
RMS

Co-RMS
EL

DE
Risk Assessment EFSA
Category HB Review Report
Remarks The original RMS was the Netherlands.
Extention of approval (Reg (EU)2018/524)
Authorisation at national level
Authorised in In progress for
BG, CY, DE, DK, EL, ES, FR, HR, IE, IT, NL, PT, RO, UK HU
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Clodinafop and its S-isomers and their salts, expressed as clodinafop (F)
    MRLs Annex II
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Skin Sens. 1 - H317
STOT RE 2 - H373 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.003 Dir 06/39  
ARfD 0.05 Dir 06/39  
AOEL 0.026 Dir 06/39  
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