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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 703/2011 Old Legislation 1998/47/EC ,
2007/21/EC ,
2010/55/EU ,
Reg. (EU) No 540/2011
Date of approval 01/01/2012 Expiration of approval 31/12/2021
RMS AT

Risk Assessment EFSA
Category FU Review Report   Confirmatory data 2015
  Renewal 2011
  Inclusion 1998
Remarks Co-RMS is Norway

The original RMS was UK.
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, MT, NL, PL, PT, RO, SE, SI, SK, UK
Classification Reg. 1272/2008
Acute Tox. 3 - H331 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.2 EFSA 2010  
ARfD Not applicable EFSA 2010  
AOEL 0.2 EFSA 2010  
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