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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 03/81/EC ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) 2016/2016 ,
Reg.(EU)2018/524
Date of approval 01/08/2004 Expiration of approval 30/04/2019
RMS

Co-RMS
IT

MT
Risk Assessment Commission
Category FU, RE Review Report
Remarks Extension of the approval period (Reg. (EU) 2018/524) The original RMS was Belgium.
Type Candidate for Substitution (CfS) CfS - criteria two PBT criteria
Authorisation at national level
Authorised in In progress for
AT, BE, CY, CZ, EL, FR, HR, HU, IT, MT, PL, PT, RO, SI, SK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Dithiocarbamates (dithiocarbamates expressed as CS2, including maneb, mancozeb, metiram, propineb, thiram and ziram)
    MRLs Annex II
  • Annex IIIB
  • Ziram
    MRLs Annex II
  • Annex IIIB
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Skin Sens. 1 - H317
Eye Dam. 1 - H318 Acute Tox. 2 - H330
STOT SE 3 - H335 STOT RE 2 - H373
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.006 Dir 03/81  
ARfD 0.08 SCoFCAH 29.6.04  
AOEL 0.015 Dir 03/81  
Other
ADI 0,003 JMPR 1996 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level