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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2011/50/EU ,
Reg. (EU) No 540/2011
   
Date of approval 01/06/2011 Expiration of approval 31/05/2021
RMS

Co-RMS
SE

BE
Risk Assessment EFSA
Category HB 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 RMS was UK.

The original Co-RMS was France.
Authorisation at national level
Authorised in In progress for
BE, DE, ES, FR, NL, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Carbetamide (sum of carbetamide and its S isomer)
    MRLs Annex II
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Carc. 2 - H351
Repr. 1B - H360D Aquatic Chronic 2 - H411
Toxicological information
Reference values Source Remark
ADI 0.06 11/50/EU  
ARfD 0.3 11/50/EU  
AOEL 0.12 11/50/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