General Information
Version
1.0, CURRENT
Revision date
2021-08-26
Product name
Esenta adhesive remover 150 ml
Product name
Esenta adhesive remover 150 ml
Identification on the label/Trade name
SDS21-056-EU
1.2.1 Relevant identified uses
The product is intended for professional use
Emergency telephone
1-866-968-6376, 1-800-465-6302, +44(0)1244 284 882, +61(0)3 9239 2700
Icons in SDS
Company Information
company name
Change Control
e-mail address of the competent person responsible for the Safety Data Sheet
stoma.webcare@convatec.com, wound.webcare@convatec.com, uk.customerservice@convatec.com
GHS Information
Signal word
Danger
Hazard Codes
Hazard statements (CLP)
H222, H229, H280
Hazard statements
Code
Statements
H222
Extremely flammable aerosol
Section 2
SECTION 2: Hazards identification
Regulation (EC) No. 1272/2008 Classification of the substance or mixture
Hazard pictograms
GHS02, GHS04
Signal word
Danger
Hazard statements
H222 Extremely flammable aerosol H229 Pressurised container: may burst if heated H280 Contains gas under pressure; may explode if heated
Precautionary statements
P210 Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking. P211 Do not spray on an open flame or other ignition source. P251 Do not pierce or burn, even after use. P410+P403 Protect from sunlight. Store in a well-ventilated place. P410+P412 Protect from sunlight. Do not expose to temperatures exceeding 50 °C/122 °F. Additional labelling according to Directive 75/324/EEC relating to aerosol dispensers Extremely flammable. Pressurized container: may burst if heated. Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking. Do not pierce or burn, even after use. Protect from sunlight. Do not expose to temperatures exceeding 50 °C/122 °F.
Other physicochemical hazards
THE PRODUCT IS FLAMMABLE!
2.1 Classification of the substance or mixture
Classification according to Regulation (EC) No 1272/2008 Additional information: According to Regulation EU 1272/2008; Article 1.5 a; Medicinal products for human use, as defined in Directive 2001/83/EC in their final state and intended for the final user, are exempted for both classification and labelling according to this Regulation Article 1.5 b; Medicinal products for veterinary use, as defined in Directive 2001/82/EC in their final state and intended for the final user, are exempted for both classification and labelling according to this Regulation. Article 1.5 d; Medical devices as defined in Directives 90/385/EEC and 93/42/EEC, which are invasive or used in direct physical contact with the human body, and in Directive 98/79/EC, are exempted for both classification and labelling according to this Regulation.
