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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
CZ

IE
Risk Assessment Commission
Category HB Review Report   List of studies relied upon (AIR 3)
  Inclusion 2003
Remarks The original RMS was France.

Extension of the approval period: Reg. (EU) 2017/1511
Authorisation at national level
Authorised in In progress for
AT, BE, CZ, DE, ES, FR, IE, LU, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Flurtamone
    MRLs Annex II
Classification Reg. 1272/2008
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.03 03/84/EC  
ARfD Not applicable 03/84/EC  
AOEL 0.02 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