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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 800/2011 Old Legislation 2008/934/EC
Date of approval 01/01/2012 Expiration of approval 31/12/2021
RMS

Co-RMS
HU

DK
Risk Assessment EFSA
Category IN Review Report   Confirmatory data 2013
  Approval 2011
Authorisation at national level
Authorised in In progress for
AT, BE, CZ, DE, DK, EL, ES, FR, HR, HU, IT, NL, PL, PT, RO, SE, SI, SK, UK BG, MT
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Tefluthrin (F)
    MRLs Annex IIIA
Classification Reg. 1272/2008
Acute Tox. 2 - H300 Acute Tox. 2 - H310
Acute Tox. 1 - H330 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.005 EFSA 10  
ARfD 0.005 EFSA 10  
AOEL 0.0015 EFSA 10  
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