21 CFR § 830.360 Unique Device Identification

§ 830.360 Records to be maintained by the labeler.

Current through Sep 8, 2026 · Read all of Part 830

(a) Each labeler shall retain, and submit to FDA upon specific request, records showing all unique device identifiers (UDIs) used to identify devices that must bear a UDI on their label, and the particular version or model associated with each device identifier. These records must be retained for 3 years from the date the labeler ceases to market the version or model.

(b) Compliance with this section does not relieve the labeler of the need to comply with recordkeeping requirements of any other FDA regulation.

← § 830.350 Correction of information submitted to the Global Unique Device Identification Database.