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Title 21 - Food and Drugs
Chapter I - FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
Subchapter H - MEDICAL DEVICES
21 CFR Part 830
21 CFR Part 830
UNIQUE DEVICE IDENTIFICATION
June 25, 2020
Subpart
A
General Provisions
Subpart
B
Requirements for a Unique Device Identifier
Subpart
C
FDA Accreditation of an Issuing Agency
Subpart
D
FDA as an Issuing Agency
Subpart
E
Global Unique Device Identification Database
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