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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2009/77/EC ,
Reg. (EU) No 540/2011
   
Date of approval 01/01/2010 Expiration of approval 31/12/2021
RMS

Co-RMS
NL

CZ
Risk Assessment EFSA
Category HB Review Report
Remarks Extension of the approval period: Reg. (EU) 2017/555

The original RMS was UK.
Type Candidate for Substitution (CfS) CfS - criteria two PBT criteria
Authorisation at national level
Authorised in In progress for
BE, FR, IE, IT, NL, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Tri-allate
    MRLs Annex IIIA
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Skin Sens. 1 - H317
STOT RE 2 - H373 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.025 Dir 09/77  
ARfD 0.6 Dir 09/77  
AOEL 0.032 Dir 09/77  
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