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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 200/2013 Old Legislation Dossier complete 2009/535
Date of approval 01/08/2013 Expiration of approval 31/07/2023
RMS

Co-RMS
DE

NL
Risk Assessment EFSA
Category FU Review Report
Remarks Corrigendum to Commission Implementing Regulation (EU) No 200/2013

The original RMS were Netherlands.
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, EE, EL, ES, FR, HR, HU, IE, IT, LT, LU, LV, MT, NL, PL, PT, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Ametoctradin (R)
    MRLs Annex IIIA
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 10 EFSA 2012  
ARfD Not applicable EFSA 2012  
AOEL 2 EFSA 2012  
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