06. November 2019
Put it simply – the new UDI-System
A straightforward overview with a practical example
Download our white paper
The white paper provides a straightforward illustration and description of the UDI System, based on a practical example.
The new EU-Regulation for medical devices (MDR) requires a unique product identification and the adherence to registration regulation.
The UDI code shall be publicly available through registration in a central database. The requirement for UDI is new and the central database is not yet available. Therefore, no practical examples and experiences are available. However, medical device manufacturers must find a way to prepare for the implementation of the UDI system.