Global Unique Device Identification Database

  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
  7. Global Unique Device Identification Database

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Section
830.300

Devices subject to device identification data submission requirements.

Section
830.310

Information required for unique device identification.

Section
830.320

Submission of unique device identification information.

Section
830.330

Times for submission of unique device identification information.

Section
830.340

Voluntary submission of ancillary device identification information.

Section
830.350

Correction of information submitted to the Global Unique Device Identification Database.

Section
830.360

Records to be maintained by the labeler.