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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 84/2018 ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 762/2013
Old Legislation 05/72/EC
Date of approval 01/07/2006 Expiration of approval 31/01/2019
RMS

Co-RMS
UK

EL
Risk Assessment Commission
Category FU Review Report
Remarks The original RMS was Italy.

Extension of the approval period (Reg(EU)84/2018)
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
  • Dithiocarbamates (dithiocarbamates expressed as CS2, including maneb, mancozeb, metiram, propineb, thiram and ziram)
    MRLs Annex II
  • Annex IIIB
Classification Reg. 1272/2008
Skin Sens. 1 - H317 Repr. 2 - H361d
Aquatic Acute 1 - H400  
Toxicological information
Reference values Source Remark
ADI 0.05 Dir 05/72  
ARfD 0.6 Dir 05/72  
AOEL 0.035 Dir 05/72  
Other
ARfD 0.006 AUS 1992, ADI 0,03 JMPR 1993 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level