21 CFR Part 830 - PART 830—UNIQUE DEVICE IDENTIFICATION
- Subpart A—General Provisions (§ 830.3)
- Subpart B—Requirements for a Unique Device Identifier (§§ 830.10 - 830.60)
- Subpart C—FDA Accreditation of an Issuing Agency (§§ 830.100 - 830.130)
- Subpart D—FDA as an Issuing Agency (§§ 830.200 - 830.220)
- Subpart E—Global Unique Device Identification Database (§§ 830.300 - 830.360)