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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2008/125 ,
Reg. (EU) 2017/195 ,
Reg. (EU) No 540/2011
   
Date of approval 01/09/2009 Expiration of approval 31/08/2022
RMS

Co-RMS
DK

LV
Risk Assessment EFSA
Category HB Review Report   Confirmatory data 2015
  Inclusion 2009
Authorisation at national level
Authorised in In progress for
AT, BE, CY, CZ, DE, DK, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, PT, RO, SE, SI, SK, UK BG, MT
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Metamitron
    MRLs Annex IIIA
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Aquatic Acute 1 - H400
Toxicological information
Reference values Source Remark
ADI 0.03 EFSA 08  
ARfD 0.1 EFSA 08  
AOEL 0.036 Dir 08/125  
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