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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 826/2013 Old Legislation 2011/123/EU
Date of approval 01/02/2014 Expiration of approval 31/01/2024
RMS

Co-RMS
FR

AT
Risk Assessment EFSA
Category FU Review Report
Authorisation at national level
Authorised in In progress for
AT, BE, CY, CZ, EE, EL, FI, FR, HU, IT, LT, LU, LV, NL, PL, RO, SE, SK, UK BG, ES, IE
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Sedaxane
    MRLs Annex IIIA
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.11 Reg. (EU) No 826/2013  
ARfD 0.3 Reg. (EU) No 826/2013  
AOEL 0.28 Reg. (EU) No 826/2013  
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