Beta Test

Medical Wire & Equipment

Revision date : 2020-09-01

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Health risk rating 1
Safety risk rating 1
Environmental risk rating 1

General Information

Revision date

2020-09-01

Product name

Beta Test

Substance name

and of the company

1.2.1 Relevant identified uses

In-vitro diagnostics under clinical supervision

1.2.2. Uses advised against

Void

Manufacturer Name

Medical Wire & Equipment

Emergency telephone

+44 1225 810361

Icons in SDS

Company Information

company name

Medical Wire & Equipment

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

sds@mwe.co.uk

GHS Information

Signal word

Void

Section 2

SECTION 2: Hazards identification

(29 CFR 1910.1200) 1.4 Emergency Telephone Number . +44 1225 810361 Classification of the substance or mixture Classification of the mixture according to Regulation 1272/2008/EC This product is not classified This product contains no hazardous constituents, or the concentration of all chemical constituents are below the regulatory threshold limits described by European directive 1272/2008/EC and the Occupational Safety Health

2.2 Label elements

The product is not subject to hazard identification regulations according to EU directives. Void

Hazard pictograms

Void

Signal word

Void

Hazard statements

Void

Results of PBT and vPvB assessment

Not applicable Section 3: Composition /information on

2.1 Classification of the substance or mixture

Classification of the mixture according to Regulation 1272/2008/EC This product is not classified This product contains no hazardous constituents, or the concentration of all chemical constituents are below the regulatory threshold limits described by European directive 1272/2008/EC and the Occupational Safety Health Administration Hazard Communication Standard 29 CFR 1910.1200 and the Canadian Workplace Hazardous Materials Information System (WHMIS). Information pertaining to particular dangers for man and environment The product presents no hazards to man or the environment as calculated by the procedures of the EU directives (1999/45/EC and Amendments)

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