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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) 2017/358 ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 974/2011
Old Legislation 2008/934
Date of approval 01/01/2012 Expiration of approval 31/12/2021
RMS

Co-RMS
FR

ES
Risk Assessment EFSA
Category AC Review Report   Review report 2017
  Acrinathrin RR Oct 2011.pdf
Authorisation at national level
Authorised in In progress for
CY, EL, ES, FR, IT, MT, PT
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Acrinathrin (F)
    MRLs Annex II
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.01 Reg. (EU) 2017/358  
ARfD 0.01 Reg. (EU) 2017/358  
AOEL 0.007 Reg. (EU) 2017/358  
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