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Reg. (EU) No 540/2011
|Date of approval||01/06/2011||Expiration of approval||31/05/2021|
Initially non included by Decision 2008/934. Included as from 1 June 2011 following re-submission for inclusion according to Reg. 33/2008.
The original RMS was UK.
The original Co-RMS was France.
Authorisation at national level
|Authorised in||In progress for|
|BE, DE, ES, FR, NL, UK|
Classification Reg. 1272/2008
|Acute Tox. 4 - H302||Carc. 2 - H351|
|Repr. 1B - H360D||Aquatic Chronic 2 - H411|
- RMS:Rapporteur Member State
- Co-RMS:Co-Rapporteur Member State
- ADI:Acceptable daily intake
- ARfD:Acute reference dose
- AOEL:Acceptable operator exposure level