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FDA Publishes Proposed UDI Rule

28 September 2012

Medical Device Alert

On 3 July 2012 the U.S. Food and Drug Administration (FDA) released its proposed rule on the Unique Device Identification (UDI) system that would apply to all medical devices (devices) minus certain categorical exceptions. The proposed rule would fulfill the statutory requirement of the FDA Amendments Act of 2007.

Read More: FDA Publishes Proposed UDI Rule


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