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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 03/84/EC ,
Reg. (EU) No 2018/1262 ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 823/2012
Old Legislation Reg. (EU) 2016/950 ,
Reg. (EU) 2017/1511
Date of approval 01/01/2004 Expiration of approval 31/10/2019
RMS

Co-RMS
PL

FR
Risk Assessment Commission
Category HB Review Report
Remarks The original RMS was France.

Extension of the approval period: Reg. (EU) 2017/1511
Type Candidate for Substitution (CfS) CfS - criteria two PBT criteria
Authorisation at national level
Authorised in In progress for
AT, BE, CY, CZ, DE, EE, EL, ES, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, PT, SI, SK, UK BG, FI, SE
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Flufenacet (sum of all compounds containing the N fluorophenyl-N-isopropyl moiety expressed as flufenacet equivalent)
    MRLs Annex II
  • Annex IIIB
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 0.005 03/84/EC  
ARfD 0.017 03/84/EC  
AOEL 0.017 03/84/EC  
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