Unique Device Identification (UDI)

System for individually labeling medical devices -

In April 2013, the European Commission issued a "Recommendation on a common framework for a single product labelling system for medical devices in the Union" and supports a UDI system with uniform functionality worldwide. The UDI recommendation of the European Commission applies to medical devices and in vitro diagnostics (IVD). In Europe, the final definition of the UDI guidelines will take place within the framework of the new EU regulation on medical devices (MDR).

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For companies that are affected by this, argus sensorsysteme offers support in the form of information, software and hardware (identification and tracking systems) for implementation as well as project support during implementation.

Do not hesitate to contact us!