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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2011/19/EU ,
Reg.(EU) No 2018/1266 ,
Reg.(EU) No 540/2011
   
Date of approval 01/06/2011 Expiration of approval 31/05/2024
RMS

Co-RMS
DK

DE
Risk Assessment EFSA
Category IN Review Report   Final Review Report 2018
  Review Report 2011
Remarks Initially non included by Decision 2008/934. Included as from 1 June 2011 following re-submission for inclusion according to Reg. 33/2008
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EE, EL, ES, FI, FR, HR, HU, IT, LT, LV, MT, PL, PT, RO, SE, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Tau-Fluvalinate (F)
    MRLs Annex IIIA
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Skin Irrit. 2 - H315
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.005 EFSA 2018  
ARfD 0.05 EFSA 2018  
AOEL 0.0044 EFSA 2018  
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