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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2010/90/EU ,
Reg. (EU) No 2018/1260 ,
Reg. (EU) No 540/2011
   
Date of approval 01/05/2011 Expiration of approval 30/04/2023
RMS

Co-RMS
CZ

BE
Risk Assessment EFSA
Category AC, IN Review Report   Confirmatory data 2016
  Inclusion 2010
Remarks Initially non included by Decision 2008/934. Inclusion voted in SCoFCAH Oct 2010 following re-submission for inclusion according to Reg. 33/2008.
Authorisation at national level
Authorised in In progress for
BE, BG, CZ, ES, FR, HU, IT, NL, PL, RO, SK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Pyridaben (F)
    MRLs Annex IIIA
Classification Reg. 1272/2008
Acute Tox. 3 - H301 Acute Tox. 3 - H331
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.01 EFSA 10  
ARfD 0.05 EFSA 10  
AOEL 0.005 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