Part 830—Unique Device Identification

1. CFR
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3. Title 21
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5. Chapter I
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7. Part 830

Subparts

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