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All medical equipment placed on the market in Europe must meet the requirements of either theMedical Devices Directive or the In Vitro Diagnostic Medical Devices Directive. Due to theimportance placed on issues of safety within the medical world the requirements of theapplicable Directive must be strictly applied by manufacturers wishing to place their products on the market in Europe.Technology International provides technical advice and support to clients whose products needto meet either of the Medical Devices Directives. Our services include offering general advice onthe scope and workings of the Directives, reviewing product designs against the requirements ofboth Directives and assistance with the preparation of compliance documentation.Our goal is to help clients find the most relevant and cost-effective methods to demonstrating
compliance to the Medical Devices Directives
● Machinery Directive
● Electromagnetic Compatibility ( EMC ) Directive
● Medical Devices Directives
● Radio & Telecommunications Terminal Equipment ( RED ) Directive
● Electrical & Electronic
● Electrical Safety Testing for Appliances and Consumer Electronics

STS INSPECTION & CERTIFICATION LIMITED

UNIT G25 WATERFRONT STUDIOS 1 DOCK ROAD LONDON UNITED KINGDOM E16 1AH


Tel : +0044 2084 323 088

Fax : +0044 2084 323 088

E-mail : STS@STS-UK.org

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