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U.S. Department of Health and Human Services

Medical Devices

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Unique Device Identification (UDI) for Postmarket Surveillance and Compliance Public Workshop, September 12-13, 2011

The Food and Drug Administration held a public workshop on the adoption, implementation, and use of unique device identifiers (UDIs) in various health-related electronic data systems. The purpose of this workshop was to engage multiple stakeholders to obtain information and comments on issues confronting the effective and efficient incorporation of UDIs into appropriate data sets, to identify barriers and incentives to their adoption and use, and to understand the best solutions and practices to resolve open issues.

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Non-FDA Presentations

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