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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) 2016/177 ,
Reg. (EU) No 540/2011
   
Date of approval 02/03/2016 Expiration of approval 02/03/2023
RMS

Co-RMS
FR

AT
Risk Assessment EFSA
Category FU Review Report
Type Candidate for Substitution (CfS) CfS - criteria two PBT criteria
Authorisation at national level
Authorised in In progress for
AT, BE, CZ, DE, EE, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, RO, SE, SI, SK, UK BG
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Benzovindiflupyr
    MRLs Annex II
Classification Reg. 1272/2008
Acute Tox. 3 - H301 Acute Tox. 3 - H331
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.05 Reg. (EU) 2016/177  
ARfD 0.1 Reg. (EU) 2016/177  
AOEL 0.04 Reg. (EU) 2016/177  
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