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Medical Device Reporting

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

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Subpart
A

General Provisions

Subpart
B

Generally Applicable Requirements for Individual Adverse Event Reports

Subpart
C

User Facility Reporting Requirements

Subpart
D

Importer Reporting Requirements

Subpart
E

Manufacturer Reporting Requirements

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