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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 06/85/EC ,
Reg. (EU) 2018/917 ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) 2015/415
Date of approval 01/08/2007 Expiration of approval 31/07/2019
RMS

Co-RMS
EL

CY
Risk Assessment EFSA
Category NE Review Report
Remarks The original RMS was the Netherlands.
Type Candidate for Substitution (CfS) CfS - criteria low ADI / ARfD / AOEL
Authorisation at national level
Authorised in In progress for
CY, EL, ES, HU, IT, MT, PT
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Fenamiphos (sum of fenamiphos and its sulphoxide and sulphone expressed as fenamiphos)
    MRLs Annex II
Classification Reg. 1272/2008
Acute Tox. 2 - H300 Acute Tox. 2 - H310
Eye Irrit. 2 - H319 Acute Tox. 2 - H330
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.0008 Dir 06/85  
ARfD 0.0025 Dir 06/85  
AOEL 0.0008 Dir 06/85  
Other
ARfD 0,003 - ADI 0,0008 JMPR 2002 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level