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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2010/92/EU ,
Reg. (EU) No 2018/670 ,
Reg. (EU) No 540/2011
   
Date of approval 01/02/2011 Expiration of approval 31/01/2024
RMS

Co-RMS
BE

CZ
Risk Assessment EFSA
Category FU Review Report   Confirmatory data 2016
  Inclusion 2010
Remarks Initially non included by Decision 2008/832. Included as from 1 February 2011 following re-submission for inclusion according to Reg. 33/2008
Type Candidate for Substitution (CfS) CfS - criteria two PBT criteria
Authorisation at national level
Authorised in In progress for
AT, BE, CZ, DE, ES, FR, HU, IE, IT, PL, SK, UK NL
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Bromuconazole (sum of diasteroisomers) (F)
    MRLs Annex IIIA
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.01 10/92/EU  
ARfD 0.1 10/92/EU  
AOEL 0.025 10/92/EU  
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