Part 830. PART 830—UNIQUE DEVICE IDENTIFICATION

• SUBPART A [§ 830.3 - § 830.3] - Subpart A—General Provisions
• SUBPART B [§ 830.10 - § 830.60] - Subpart B—Requirements for a Unique Device Identifier
• SUBPART C [§ 830.100 - § 830.130] - Subpart C—FDA Accreditation of an Issuing Agency
• SUBPART D [§ 830.200 - § 830.220] - Subpart D—FDA as an Issuing Agency
• SUBPART E [§ 830.300 - § 830.360] - Subpart E—Global Unique Device Identification Database