PLANTS

Language selector

Accessibility tools

Navigation path

Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 350/2013 Old Legislation 2012/363/EU ,
Dossier complete 2009/700/EC
Date of approval 01/10/2013 Expiration of approval 30/09/2023
RMS

Co-RMS
CZ

BE
Risk Assessment EFSA
Category FU Review Report
Remarks The original RMS was UK.
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CZ, DE, EE, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, PT, RO, SE, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Bixafen (R)
    MRLs Annex IIIA
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.02 EFSA 2012  
ARfD 0.2 EFSA 2012  
AOEL 0.13 EFSA 2012  
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