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New EU Regulation on Medical Devices (MDR)
Nordic activity AB meets the requirements of the new European Medical Technology Regulation EU 2017/745 (MDR), which entered into force on 26 May 2021 and which replaces the previous MDD directive.
That Nordic activity AB meets the requirements of the MDR regulation is a confirmation that our products are safe to use and of good quality for patients, users and our customers.
Request declaration of conformity via e-mail email@example.com