General Information
Version
2.0
Product name
Inter Dry Europe
Manufacturer Name
Coloplast A/S
Emergency telephone
+45 82 12 12 12, 1-800-222-1222, 1-877-820-7008
Icons in SDS
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
1272/2008 This product is regulated as a medical device in the European Economic Area (EEA). In other regions it may be regulated as a medical device, a cosmetic or not regulated. The product is assessed and supplied with a safety data
2.2 Label elements
The product is a medical device in EAA and therefore the labelling elements from the CLP regulations do not apply, according to Regulation (EC) No
2.3 Other hazards
Assessment to determine PBT and vPvB has not been made
2.1 Classification of the substance or mixture
Classification according to Regulation (EC) No 1272/2008: Not classified Wording of H-statements – see section 16.
