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Medical Device Reporting
Law
CFR 21
Food and Drugs
Food and Drug Administration, Department of Health and Human Services
Medical Devices
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