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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2010/14/EU ,
Reg. (EU) 2017/1527 ,
Reg. (EU) No 540/2011
   
Date of approval 01/06/2010 Expiration of approval 31/05/2021
RMS

Co-RMS
FR

ES
Risk Assessment EFSA
Category EL Review Report
Remarks Extension of approval period: Reg. (EU) 2017/1527
Authorisation at national level
Authorised in In progress for
FR
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Heptamaloxyloglucan
    MRLs Annex IV
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI Not applicable EFSA ´09  
ARfD Not applicable EFSA ´09  
AOEL Not applicable EFSA ´09  
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