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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 05/53/EC ,
Reg. (EU) No 540/2011 ,
Reg.(EU) No 2018/1262
Old Legislation Reg. (EU) No 2017/1511 ,
Reg. (EU) No 533/2013
Date of approval 01/03/2006 Expiration of approval 31/10/2019
RMS

Co-RMS
CZ

HU
Risk Assessment Commission
Category PG Review Report
Remarks The original RMS was the Netherlands.

Extension of approval period: Reg. (EU) 2017/1511
Authorisation at national level
Authorised in In progress for
AT, BE, CY, CZ, DE, DK, EL, ES, FI, FR, HU, IE, IT, NL, PL, PT, SE, SI, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Daminozide (sum of daminozide and 1,1-dimethyl-hydrazine (UDHM), expressed as daminozide)
    MRLs Annex V
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.45 Dir 05/53  
ARfD Not applicable Dir 05/53  
AOEL 0.16 Dir 05/53  
Other
ADI 0,5 JMPR 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