FDA To Open GUDID Accounts For Class III I/LS/LS Devices Jan. 26

The massive Global Unique Identifier Database that tracks medical devices will open for labelers of Class III implantable, life-supporting, life-sustaining devices on Monday, Jan. 26, the agency announced in a webinar on Wednesday (Jan. 14). Stakeholders have been in a holding pattern since the final UDI rule went into effect for Class III I/LS/LS in September of last year. The announcement from FDA came in the middle of a webinar guiding stakeholders on GUDID submissions, an effort by the agency...

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