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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 05/54/EC ,
Reg. (EU) No 2018/1262 ,
Reg. (EU) No 2018/1913 ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) No 2017/1511 ,
Reg. (EU) No 533/2013
Date of approval 01/03/2006 Expiration of approval 31/10/2019
RMS

Co-RMS
SE

LV
Risk Assessment EFSA
Category HB Review Report   List of studies 2017
  list_tribenuron.pdf
Remarks Reg. (EU) 2018/1913 shall apply from 1 February 2019.
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
  • Tribenuron-methyl
    MRLs Annex II
  • Annex IIIB
Classification Reg. 1272/2008
Skin Sens. 1 - H317 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.01 Dir 05/54  
ARfD 0.2 Dir 05/54  
AOEL 0.07 Dir 05/54  
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