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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 03/84/EC ,
Reg. (EU) 2018/710 ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) 2016/950 ,
Reg. (EU) 2017/1511 ,
Reg. (EU) No 823/2012
Date of approval 01/07/2018 Expiration of approval 30/06/2033
RMS

Co-RMS
IE

BE
Risk Assessment EFSA
Category FU Review Report   Renewal Report 2018
  List of studies 2016
  Inclusion 2003
Authorisation at national level
Authorised in In progress for
BE, CZ, DE, DK, EE, ES, FR, IE, IT, LT, LU, LV, NL, PL, SE, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Silthiofam
    MRLs Annex II
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.05 Reg. (EU) 2018/710  
ARfD 0.2 Reg. (EU) 2018/710  
AOEL 0.1 Reg. (EU) 2018/710  
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