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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 05/2/EC ,
Reg. (EU) 2018/917 ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) 2017/841
Date of approval 01/04/2005 Expiration of approval 31/07/2019
RMS

Co-RMS
HU

NL
Risk Assessment Commission
Category FU Review Report
Remarks The original RMS was Finland.
Authorisation at national level
Authorised in In progress for
AT, BE, CY, DE, EE, ES, FI, FR, IE, NL, PL, SE, SI, UK HU
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Gliocladium catenulatum strain J1446 (++)
    MRLs Annex IV
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI Not applicable 05/2/EC  
ARfD Not applicable 05/2/EC  
AOEL Not applicable 05/2/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