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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 375/2013 Old Legislation 2011/252/EU ,
Dossier complete 03/105/EC
Date of approval 01/10/2013 Expiration of approval 30/09/2023
RMS

Co-RMS
IT

AT
Risk Assessment EFSA
Category AC, IN Review Report
Remarks The original RMS was UK.
Authorisation at national level
Authorised in In progress for
BE, CY, EL, ES, FR, HU, IT, LU, MT, NL IE
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Spiromesifen
    MRLs Annex IIIA
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.03 EFSA 07  
ARfD 2 EFSA 07  
AOEL 0.015 EFSA 07  
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