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Part 830
FEDERAL · 21 CFR
Part 830 — Unique Device Identification
20 sections · Title 21: Food and Drugs
§ 830.3
Definitions.
§ 830.10
Incorporation by reference.
§ 830.20
Requirements for a unique device identifier.
§ 830.40
Use and discontinuation of a device identifier.
§ 830.50
Changes that require use of a new device identifier.
§ 830.60
Relabeling of a device that is required to bear a unique device identifier.
§ 830.100
FDA accreditation of an issuing agency.
§ 830.110
Application for accreditation as an issuing agency.
§ 830.120
Responsibilities of an FDA-accredited issuing agency.
§ 830.130
Suspension or revocation of the accreditation of an issuing agency.
§ 830.200
When FDA will act as an issuing agency.
§ 830.210
Eligibility for use of FDA as an issuing agency.
§ 830.220
Termination of FDA service as an issuing agency.
§ 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.