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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2011/25/EU ,
Reg. (EU) No 2018/1266 ,
Reg. (EU) No 540/2011
   
Date of approval 01/06/2011 Expiration of approval 31/05/2024
RMS

Co-RMS
NL

PL
Risk Assessment EFSA
Category FU Review Report
Remarks Initially non included by Decision 2008/934. Included as from 1 June 2011 following re-submission for inclusion according to Reg. 33/2008

The original Co-RMS was UK.
Authorisation at national level
Authorised in In progress for
AT, CY, EL, ES, FR, HR, HU, IE, IT, MT, NL, PL, PT, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Bupirimate
    MRLs Annex IIIA
Classification Reg. 1272/2008
Skin Sens. 1B - H317 Carc. 2 - H351
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.05 EFSA 10  
ARfD Not applicable EFSA 10  
AOEL 0.05 EFSA 10  
Other
AOEL Semichronic: 0,15 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level