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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2007/76 ,
Reg. (EU) No 2018/1262 ,
Reg. (EU) No 540/2011
   
Date of approval 01/11/2008 Expiration of approval 31/10/2019
RMS

Co-RMS
FR

ES
Risk Assessment EFSA
Category FU Review Report
Remarks The original RMS was Denmark.
Type Candidate for Substitution (CfS) CfS - criteria two PBT criteria
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
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.37 Dir 07/76  
ARfD Not applicable Dir 07/76  
AOEL 0.59 Dir 07/76  
Other
ADI 0,4 ARfD not necessary (JMPR 2004) 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level