Udi device identifier. A unique device identifier (UDI) is a unique numeric or alphanumeric code that generally consists of the following: Device identifier (DI), a mandatory, fixed portion of a UDI that Include a unique device identifier (UDI), issued under an FDA-accredited issuing agency's UDI system, on device labels, device packages, and in some instances, directly on the device. Aug 21, 2023 ยท The Global Unique Device Identification Database (GUDID) contains key device identification information submitted to the FDA about medical devices that have Unique Device Identifiers (UDI). The objective is to unambiguously identify all medical devices in the healthcare supply chain through distribution and use. . Regulatory agencies increasingly require a unique device identifier (UDI) to ensure a medical device has future traceability to a manufacturer. AccessGUDID is a searchable database of device identification information, such as the device identifier on the label, device name, company name, MR safety status, Global Medical Device The unique device identification (UDI) is a unique numeric or alphanumeric code related to a medical device. Include a unique device identifier (UDI), issued under an FDA-accredited issuing agency's UDI system, on device labels, device packages, and in some instances, directly on the device. A unique device identifier (UDI) is a unique numeric or alphanumeric code that generally consists of the following: Device identifier (DI), a mandatory, fixed portion of a UDI that Include a unique device identifier (UDI), issued under an FDA-accredited issuing agency's UDI system, on device labels, device packages, and in some instances, directly on the device. It allows for a clear and unambiguous identification of specific devices on the market and facilitates their traceability. Submit device information to the Global Unique Device Identification Database (GUDID). sopxrggpsmuisboozylbsiuenxdljorclwrqyhjntzcgwbkdf