Unique Device Identification

  1. Law
  2. CFR 21
  3. Food and Drugs
  4. Food and Drug Administration, Department of Health and Human Services
  5. Medical Devices
  6. Unique Device Identification

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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