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.