Just scan to check that your device’s Unique Device Identifier (UDI) is in the FDA’s database and to track all your medical devices.
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What Are UDIS? As of September 24, 2016 all class II medical devices sold in the USA must bear a Unique Device Identifier or UDI. A UDI is an alphanumeric code in unique human readable or machine readable code.
What codes can you read? UDI Check is compatible with multiple code formats and UDI’s from all three accredited issuing agencies:
- GS1
- Health Industry Business Communications Council (HIBCC),
- International Council for Commonality in Blood Banking Automation (ICCBBA)