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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2008/113 ,
Reg. (EU) No 540/2011
   
Date of approval 01/05/2009 Expiration of approval 30/04/2019
RMS

Co-RMS
DK

NL
Risk Assessment EFSA
Category IN Review Report   Strains_SA1_SA12_EG2348_revised 2013
  Strain_ABTS351_revised 2013
  Strain PB54_revised 2013
Remarks Substance fulfilling criteria Annex VI Reg. 2229/2004
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EL, ES, FR, HR, HU, IE, IT, LT, LU, NL, PL, PT, RO, SE, SI, SK, UK MT
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Default MRL of 0.01 mg/kg according to Art 18(1)(b) Reg 396 / 2005.
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI Not applicable Dir 08/113  
ARfD Not applicable Dir 08/113  
AOEL Not applicable Dir 08/113  
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