Product Testing and Certification

SIQ is a notified body under the new Medical Devices Regulation

01. July 2022

The medical device market accounts for more than a quarter of the global market. This is a sector that is constantly and rapidly evolving and requires constant adaptation by all stakeholders. The human population is aging, which is why rehabilitation aids are gaining in importance, which, like medical aids, are becoming increasingly technologically complex, as well as the testing and certification we carry out.

As a professional, independent, and impartial institution, SIQ enables manufacturers of medical devices to place safe devices on the market that comply with European regulations. In addition to providing services for the automotive industry, the certification of medical devices is one of our strategic activities. In March this year, we became a notified body under the new Medical Devices Regulation.
More information:
Ana Pribaković Borštnik
Tel.: +386 1 4778 153

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