PLANTS

Language selector

Accessibility tools

Navigation path

Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2011/4/EU ,
Reg.(EU) No 2018/1266 ,
Reg.(EU) No 540/2011
   
Date of approval 01/06/2011 Expiration of approval 31/05/2023
RMS

Co-RMS
NL

DK
Risk Assessment EFSA
Category HB Review Report   Confirmatory data 2014
  Inclusion 2010
Remarks Initially non included by Decision 2008/934. Included as from 1 June 2011 following re-submission for inclusion according to Reg. 33/2008
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, PT, RO, SE, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Cycloxydim including degradation and reaction products which can be determined as 3-(3-thianyl)glutaric acid S-dioxide (BH 517-TGSO2) and/or 3-hydroxy-3-(3-thianyl)glutaric acid S-dioxide (BH 517-5-OH-TGSO2) or methyl esters thereof, calculated in total as cycloxydim
    MRLs Annex IIIA
Classification Reg. 1272/2008
Repr. 2 - H361d
Toxicological information
Reference values Source Remark
ADI 0.07 EFSA 10  
ARfD 2 EFSA 10  
AOEL 0,1 EFSA 10  
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