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Home Resources Commercial Resources Unique Device Identification For Medical Devices How to construct the UDI from products labeled prior to the UDI deadline

How to construct the UDI from products labeled prior to the UDI deadline

Click here to learn more about Healthcare UDI from GS1.

Click here to learn more about Medical Device/UDI from the US Food & Drug Administration (FDA).

Click here to review guidance from the FDA on the Global UDI Database (GUDID).

Click here to access the FDA's Global Unique Device Identification Database (GUDID).

Click here to visit the global GS1 website.

Click here to visit the GS1 United States website.

For further questions regarding Smith+Nephew’s electronic product data, please contact us at PDSC.Global@smith-nephew.com

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