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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2011/6/EU ,
Reg. (EU) 2017/360 ,
Reg. (EU) 2018/670 ,
Reg. (EU) No 540/2011
Old Legislation 2008/771/EC
Date of approval 01/02/2011 Expiration of approval 31/01/2023
RMS

Co-RMS
IT

AT
Risk Assessment EFSA
Category AC, IN Review Report   Review report 2017
  Inclusion 2010
Remarks FI was the original RMS
Authorisation at national level
Authorised in In progress for
BE, CZ, DK, ES, FI, IT, NL, PT, SI, UK AT, BG, HU
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Buprofezin (F)
    MRLs Annex IIIA
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.01 Reg. (EU) 2017/360  
ARfD 0.5 Reg. (EU) 2017/360  
AOEL 0.04 Reg. (EU) 2017/360  
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