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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 00/80/EC ,
Reg. (EU) 2016/146 ,
Reg. (EU) No 540/2011
Old Legislation 2010/77/EU ,
Reg. (EU) 2015/1885
Date of approval 01/04/2016 Expiration of approval 31/03/2023
RMS

Co-RMS
SE

FR
Risk Assessment EFSA
Category IN Review Report   Renewal 2016
  List of studies relied upon (AIR 2)
  Inclusion 2001
Type Candidate for Substitution (CfS) CfS - criteria low ADI / ARfD / AOEL, two PBT criteria
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, MT, NL, PL, PT, RO, SE, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Lambda-Cyhalothrin (F) (R)
    MRLs Annex II
Classification Reg. 1272/2008
Acute Tox. 3 - H301 Acute Tox. 4 - H312
Acute Tox. 2 - H330 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.0025 Reg. (EU) 2016/146  
ARfD 0.005 Reg. (EU) 2016/146  
AOEL 0.00063 Reg. (EU) 2016/146  
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