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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2009/11 ,
Reg. (EU) No 540/2011
   
Date of approval 01/11/2009 Expiration of approval 31/10/2022
RMS

Co-RMS
FR

BE
Risk Assessment EFSA
Category AC Review Report   Inclusion 2008
  Confirmatory data 2012
Remarks Extension of the approval period: Reg. (EU) 2017/555
Type Candidate for Substitution (CfS) CfS - criteria two PBT criteria
Authorisation at national level
Authorised in In progress for
BE, BG, CY, CZ, DE, EL, FR, HR, HU, IE, IT, LU, NL, PL, PT, SI, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Tebufenpyrad (F)
    MRLs Annex II
Classification Reg. 1272/2008
Acute Tox. 3 - H301 Skin Sens. 1B - H317
Acute Tox. 4 - H332 STOT RE 2 - H373
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.01 Dir 09/11  
ARfD 0.02 Dir 09/11  
AOEL 0.01 Dir 09/11  
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