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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) 2016/370 ,
Reg. (EU) No 289/2014 ,
Reg. (EU) No 540/2011
Old Legislation 2005/459/EC ,
2012/191/EU
Date of approval 01/07/2016 Expiration of approval 30/06/2026
RMS UK

Risk Assessment EFSA
Category HB Review Report
Remarks Provisional authorisations extended until 31/05/2016.
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, EE, EL, ES, FI, FR, HR, HU, IT, LT, LU, LV, NL, PL, PT, RO, SI, SK, UK IE, SE
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Pinoxaden
    MRLs Annex IIIA
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.1 Reg. (EU) 2016/370  
ARfD 0.1 Reg. (EU) 2016/370  
AOEL 0.1 Reg. (EU) 2016/370  
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