Laser marking in accordance with the UDI
The Medical Device Regulation (MDR) changed the requirements for manufacturers that develop medical devices for the Euro…
The Medical Device Regulation (MDR) changed the requirements for manufacturers that develop medical devices for the Euro…
TÜV Rheinland LGA Products GmbH is now a notified body for the EU Medical Device Regulation (MDR) 2017/745. The European…
. Introduction The MDR (Medical Device Regulation) is currently a hot topic and is keeping manufacturers of medical pr…