Woun’Dres

Coloplast A/S

Revision date : 2016-09-22

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General Information

Version

2.0

Revision date

2016-09-22

Product name

Woun’Dres

Manufacturer Name

Coloplast A/S

Emergency telephone

+45 82 12 12 12, 1-800-222-1222, 1-877-820-7008

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Company Information

company name

Coloplast A/S

e-mail address of the competent person responsible for the Safety Data Sheet

msds@coloplast.com

Section 2

SECTION 2: Hazards identification

Regulation (EC) No. 1272/2008 The product is a medical device and therefore not covered by the classifica- tion and labelling rules that apply to chemical products. This safety data sheet is supplied as an additional service to the customer. Classification of the substance or mixture The product is a medical device product and therefore not covered by the classification and labelling rules that apply to chemical products according to

2.2 Label elements

The product is a medical device product and therefore the labelling elements from the CLP regulations

2.3 Other hazards

Assessment to determine PBT and vPvB has not been made (not required).

2.1 Classification of the substance or mixture

The product is a medical device product and therefore not covered by the classification and labelling rules that apply to chemical products according to i.e. Regulation (EC) No 1272/2008.

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Employee access – Tablets, Smartphones, or link from Corporate Intranet
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Safety – One-click access to first aid information.
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Labels – Generate Secondary Container Labels with just one click.