PLANTS

Language selector

Accessibility tools

Navigation path

Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 03/84/EC ,
Reg (EU) No 2018/1917 ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) 2016/950 ,
Reg. (EU) 2017/1511 ,
Reg. (EU) No 2018/1262 ,
Reg. (EU) No 823/2012
RMS

Co-RMS
CZ

IE
Risk Assessment EFSA
Category HB Review Report   Review Report 2018
  List of studies relied upon (AIR 3)
  Inclusion 2003
Remarks The original RMS was France.
Non-renewal of approval voted in October 2018.
Withdrawal authorisations by 27 June 2019.
Max period of grace:27 March 2020.

Authorisation at national level
Authorised in In progress for
AT, BE, CZ, DE, DK, 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 Reg (EU) No 2018/1917 Provisional 
ARfD 0.5 Reg (EU) No 2018/1917 Provisional 
AOEL 0.05 Reg (EU) No 2018/1917 Provisional 
Other
AAOEL 0.17 mg/kg/bw - provisional 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level