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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 03/5/EC ,
Reg. (EU) No 2018/1262 ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 823/2012
Old Legislation Reg. (EU) 2016/950 ,
Reg. (EU) 2017/1511
Date of approval 01/11/2003 Expiration of approval 31/10/2019
RMS

Co-RMS
UK

AT
Risk Assessment Commission
Category IN Review Report
Remarks The original RMS was Sweden.

Extension of the approval period: Reg. (EU) 2017/1511
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
  • Deltamethrin (cis-deltamethrin) (F)
    MRLs Annex II
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 Dir 03/5  
ARfD 0.01 Dir 03/5  
AOEL 0.0075 Dir 03/5  
Other
ADI 0,01 ARfD 0,05 JMPR 2000 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level