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 info@nordicactivity.se