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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 03/84/EC ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 823/2012 ,
reg. (EU) 2018/1262
Old Legislation Reg. (EU) 2016/950 ,
Reg. (EU) 2017/1511
Date of approval 01/01/2004 Expiration of approval 31/10/2019
RMS

Co-RMS
DE

EL
Risk Assessment Commission
Category NE Review Report
Remarks The original RMS was the UK.

Extension of the approval period: Reg. (EU) 2017/1511
Authorisation at national level
Authorised in In progress for
BE, BG, CY, DE, EL, ES, FR, HR, HU, IE, IT, MT, NL, PL, RO, UK AT
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Fosthiazate
    MRLs Annex II
  • Annex IIIB
Classification Reg. 1272/2008
Acute Tox. 3 - H301 Acute Tox. 4 - H312
Skin Sens. 1 - H317 Acute Tox. 3 - H331
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.004 03/84/EC  
ARfD 0.005 03/84/EC  
AOEL 0.005 03/84/EC  
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