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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 03/23/EC ,
Reg. (EU) 2018/917 ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 823/2012
Old Legislation Reg. (EU) 2016/950 ,
Reg. (EU) 2017/841
Date of approval 01/07/2003 Expiration of approval 31/07/2019
RMS

Co-RMS
FR

LV
Risk Assessment Commission
Category FU Review Report   List of studies relied upon (AIR 3)
  Inclusion 2002
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EE, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, MT, NL, PL, PT, RO, SE, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Cyazofamid
    MRLs Annex II
Classification Reg. 1272/2008
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.17 03/23/EC  
ARfD Not applicable 03/23/EC  
AOEL 0.3 03/23/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