PLANTS

Language selector

Accessibility tools

Navigation path

Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2008/107 ,
Reg. (EU) 2017/438 ,
Reg. (EU) No 540/2011
   
Date of approval 01/05/2009 Expiration of approval 30/04/2019
RMS

Co-RMS
AT

MT
Risk Assessment EFSA
Category AC, IN Review Report   Addendum to Review Report 2017
  Inclusion 2008
  Confirmatory data 2012
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
  • Abamectin (sum of avermectin B1a, avermectin B1b and delta-8,9 isomer of avermectin B1a, expressed as avermectin B1a) (F) (R)
    MRLs Annex II
Classification Reg. 1272/2008
Acute Tox. 2 - H300 Acute Tox. 1 - H330
Repr. 2 - H361d STOT RE 1 - H372
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.0025 Dir 08/107  
ARfD 0.005 Dir 08/107  
AOEL 0.0025 Dir 08/107  
Other
ADI 0,002 JMPR 1997 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level