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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2010/25/EU ,
Reg. (EU) No 540/2011
   
Date of approval 01/08/2010 Expiration of approval 31/07/2020
RMS

Co-RMS
AT

NL
Risk Assessment EFSA
Category AC, IN Review Report
Remarks Extension provisional authorisation (2009/579)
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, DE, EE, EL, FI, FR, HR, HU, IT, LT, LU, LV, NL, PL, PT, RO, SI, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Spirodiclofen (F)
    MRLs Annex IIIA
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.015 EFSA ´09  
ARfD Not applicable EFSA ´09  
AOEL 0.009 EFSA ´09  
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