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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) 2018/1043 Old Legislation 03/68/EC ,
Reg. (EU) 2016/950 ,
Reg. (EU) 2017/841 ,
Reg. (EU) 2018/917 ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 823/2012
RMS

Co-RMS
CZ

FR
Risk Assessment EFSA
Category FU Review Report   Non-renewal 2018
  List of studies relied upon (AIR 3)
  Inclusion 2003
Remarks Non renewal voted in June 2018.
Withdrawal authorisations by 14 February 2019.
Max period of grace: 14 November 2019.
Authorisation at national level
Authorised in In progress for
BE, BG, CY, CZ, DE, DK, EE, EL, ES, FI, FR, HR, IE, IT, LT, LU, LV, NL, PL, PT, RO, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Fenamidone
    MRLs Annex II
Classification Reg. 1272/2008
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.03 03/68/EC  
ARfD Not applicable 03/68/EC  
AOEL 0.3 03/68/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