Getinge announces first manufacturing site and products to be EU MDR certified
The new European law, EU medical device regulation (EU MDR), will be fully effective in May 2020 with a transition period until May 2024. Getinge drives a focused program to ensure selected manufacturing sites and products reaches compliance with it. In February 2020, the Solna factory in Sweden along with the intensive care unit ventilators Servo-u and Servo-n was first out of the bunch to receive the certificate.An important step for Getinge to make the journey for reaching compliance with the new European law streamlined and predictable, has been to transfer selected manufacturing sites