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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 08/44/EC ,
Reg. (EU) 2018/917 ,
Reg. (EU) 540/2011
   
Date of approval 01/08/2008 Expiration of approval 31/07/2019
RMS

Co-RMS
UK

FR
Risk Assessment EFSA
Category FU Review Report
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CZ, DE, DK, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, PT, RO, SE, SI, SK, UK
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.01 08/44/EC  
ARfD 0.01 08/44/EC  
AOEL 0.2 08/44/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