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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2008/108 ,
Reg. (EU) No 540/2011
   
Date of approval 01/03/2009 Expiration of approval 28/02/2019
RMS

Co-RMS
AT

DK
Risk Assessment EFSA
Category FU Review Report
Authorisation at national level
Authorised in In progress for
AT, BE, CY, CZ, DE, DK, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, PT, RO, SE, SI, SK, UK BG
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Fluazinam (F)
    MRLs Annex II
Classification Reg. 1272/2008
Skin Sens. 1A - H317 Eye Dam. 1 - H318
Acute Tox. 4 - H332 Repr. 2 - H361d
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.01 Dir 08/108  
ARfD 0.07 Dir 08/108  
AOEL 0.004 Dir 08/108  
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