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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2009/77/EC ,
Reg. (EU) No 540/2011
   
Date of approval 01/01/2010 Expiration of approval 31/12/2019
RMS

Co-RMS
ES

HU
Risk Assessment EFSA
Category IN Review Report
Type Candidate for Substitution (CfS) CfS - criteria two PBT criteria
Authorisation at national level
Authorised in In progress for
CY, EL, ES, HR, HU, IT, MT, NL, PT, RO
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Lufenuron (any ratio of constituent isomers) (F)
    MRLs Annex II
Classification Reg. 1272/2008
Skin Sens. 1 - H317 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.015 Dir 09/77  
ARfD Not applicable Dir 09/77  
AOEL 0.01 Dir 09/77  
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