CFR /  Title 21  /  Part 830: Unique Device Identification

Section No.	Description
Section 830.3	Incorporation by reference
Section 830.10	Requirements for a unique device identifier
Section 830.20	Use and discontinuation of a device identifier
Section 830.40	Changes that require use of a new device identifier
Section 830.50	Relabeling of a device that is required to bear a unique device identifier
Section 830.60	FDA accreditation of an issuing agency
Section 830.100	Application for accreditation as an issuing agency
Section 830.110	Responsibilities of an FDA-accredited issuing agency
Section 830.120	Suspension or revocation of the accreditation of an issuing agency
Section 830.130	When FDA will act as an issuing agency
Section 830.200	Eligibility for use of FDA as an issuing agency
Section 830.210	Termination of FDA service as an issuing agency
Section 830.220	Devices subject to device identification data submission requirements
Section 830.300	Information required for unique device identification
Section 830.310	Submission of unique device identification information
Section 830.320	Times for submission of unique device identification information
Section 830.330	Voluntary submission of ancillary device identification information
Section 830.340	Correction of information submitted to the Global Unique Device Identification Database
Section 830.350	Records to be maintained by the labeler
Section 830.360	Scope