Digiterm is MDR compliant!

Being active on the market of medical devices for 30 years, Digiterm Ltd. is committed to comply all the highest requirements of healthcare applications. As you are aware, as of the end of May 2021 a new Medical Device Regulation is to be introduced by the European Commission under the number (EU) 2017/745 (MDR).

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We work as a united team around the world and give our clients the highest quality products and solutions possible. Our sales team will be happy to help you!