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FDA/CDRH Memo to the Division of Dockets Management Submission of Device Information (DI)…

Supporting & Related Material · FDA-1992-S-0039 · posted Dec 2, 2013

Key facts

Document ID FDA-1992-S-0039-0060
Title FDA/CDRH Memo to the Division of Dockets Management Submission of Device Information (DI) record to the Global Unique Device Identification Database (GUDID), in compliance with the Unique Device Identification Rule - Memorandum
Document type Supporting & Related Material
Subtype Background Material
Agency FDA
Docket FDA-1992-S-0039
Posted Dec 2, 2013

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