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Procedure for Certification of Medical Devices in Accordance with the Regulation (EU) 2017/745 on Medical Devices (MDR)

The path for the entry of a medical device to the market starts with an idea and leads through its production and testing to the eventual certification. It is recommended that the manufacturer contact the notified body already at the development s...

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SIQ is a notified body under the new Medical Devices Regulation

01. July 2022 Product Testing and Certification

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 rehabilitat...