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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2011/42/EU ,
Reg. (EU) 2018/1266 ,
Reg. (EU) No 540/2011
   
Date of approval 01/06/2011 Expiration of approval 31/05/2024
RMS

Co-RMS
SK

CZ
Risk Assessment EFSA
Category FU Review Report
Remarks Initially non included by Decision 2008/934. Included as from 1 June 2011 following re-submission for inclusion according to Reg. 33/2008.

The original Co-RMS was UK.
Authorisation at national level
Authorised in In progress for
BG, CZ, EL, ES, FR, HR, HU, IE, IT, PL, RO, UK
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.01 11/42/EU  
ARfD 0.05 11/42/EU  
AOEL 0.05 11/42/EU  
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