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Regulations last checked for updates: May 14, 2025
Title 21 - Food and Drugs last revised: May 12, 2025
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
authority:
21 U.S.C. 321
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331
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352
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353
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360
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360
d,
360
i,
360
j,
371
source:
78 FR 58823, Sept. 24, 2013, unless otherwise noted.
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