All medical devices made by TECHNOLOGIE MEDICALE comply with European directive 93/42/EEC. Compliance is verified every year by the French notified body LNE/G-MED. Accordingly, all our products carry the CE marking.
In addition, our quality management system is ISO 13485:2016 certified.
TECHNOLOGIE MEDICALE is actively engaged its industry, which is why we are a member of the leading medtech industry organisation, SNITEM (French Syndicate for the Medical Technology Industry).
To ensure all our devices function correctly, we control every product individually before it is shipped from our premises.
Every medical device bears a unit serial number, so it can be traced from the factory to your doorstep, and for the rest of its lifespan thereafter.
Our comprehensive in-house procedures mean we are able to guarantee
the reliability of our products and ensure customer satisfaction.
Please get in touch to get more information