Part 830 — Unique Device Identification
Subpart A — General Provisions
Subpart B — Requirements for a Unique Device Identifier
Subpart C — FDA Accreditation of an Issuing Agency
Subpart D — FDA as an Issuing Agency
Subpart E — Global Unique Device Identification Database
- § 830.300— Devices subject to device identification data submission requirements.
- § 830.310— Information required for unique device identification.
- § 830.320— Submission of unique device identification information.
- § 830.330— Times for submission of unique device identification information.
- § 830.340— Voluntary submission of ancillary device identification information.
- § 830.350— Correction of information submitted to the Global Unique Device Identification Database.
- § 830.360— Records to be maintained by the labeler.