https://fdalisting.com/page/10....4/us-fda-global-devi
The UDI system was established by the FDA to uniquely identify medical devices throughout their distribution and use. Each device is assigned a specific code that includes information such as the device identifier, production identifier, and manufacturer information. This information is then uploaded to the GUDID, a publicly searchable database that allows healthcare providers and patients to access important information about each device.