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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 04/58/EC ,
Reg. (EU) 2018/917 ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) 2017/841
Date of approval 01/03/2005 Expiration of approval 31/07/2019
RMS

Co-RMS
FI

DK
Risk Assessment Commission
Category HB Review Report   List of studies
  Review report 2004
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, NL, PL, PT, RO, SE, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Phenmedipham
    MRLs Annex II
Classification Reg. 1272/2008
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.03 Dir 04/58  
ARfD Not applicable Dir 04/58  
AOEL 0.13 Dir 04/58  
Other
ARfD 0.01 AUS 1991 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level