PLANTS

Language selector

Accessibility tools

Navigation path

Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 806/2011 Old Legislation 2008/934/EC
Date of approval 01/01/2012 Expiration of approval 31/12/2021
RMS

Co-RMS
CZ

SK
Risk Assessment EFSA
Category FU Review Report
Remarks The original RMS was UK.
Type Candidate for Substitution (CfS) CfS - criteria low ADI / ARfD / AOEL, two PBT criteria
Authorisation at national level
Authorised in In progress for
AT, EL, PT, RO
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Fluquinconazole (F)
    MRLs Annex IIIA
Classification Reg. 1272/2008
Acute Tox. 3 - H301 Acute Tox. 4 - H312
Skin Irrit. 2 - H315 Acute Tox. 3 - H331
STOT RE 1 - H372 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.002 EFSA 11  
ARfD 0.02 EFSA 11  
AOEL 0.001 EFSA 11  
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