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U.S. Code of Federal Regulations
Regulations most recently checked for updates: May 28, 2023
All Titles
Title 21
Chapter I
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
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