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Home » Panel Lauds UDI, But Worries About Enforcement, Other Details
Panel Lauds UDI, But Worries About Enforcement, Other Details
August 3, 2012
The FDA last week got a preview of the comments it can expect in response to its unique device identifier (UDI) draft rule ranging from whether a change in UDI would require a new supplemental PMA or 510(k) to questions about date formatting required by the rule.