The UDI is a system for uniform product marking of medical devices that is intended to increase patient safety, simplify product recalls and thus optimize market surveillance.
The UDI system originated in the USA and is now also being implemented in Europe, where the regulatory requirements are governed by the new Medical Device Regulation (MDR for short).
To meet the requirements regarding direct marking of reusable medical devices, our instruments are provided with corrosion-resistant laser marking incl. UDI code in GS1 data matrix format.
For our validated laser markings, we rely on state-of-the-art technologies that ensure a long-lasting marking.