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# Info Collection Extension for UDI System
- URL: https://www.fdaweb.com/info-collection-extension-for-udi-system/
- Published: 2019-07-31T12:00:00.000Z
- Updated: 2026-09-15T01:41:05.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5144656

*Federal Register* notice: FDA is seeking comments on an information collection extension for “Unique Device Identification (UDI) System — 21 CFR Parts 16, 801, 803, 806, 810, 814, 820, 821, 822, and 830” (OMB Control Number 0910-0720). Medical device labelers, unless excepted, are required to design and use medical device labels and device packages that bear a UDI, present dates on labels in a particular format, and submit data concerning each version or model of a device to the Global Unique Device Identification Database (GUDID) no later than the date the label of the device must bear a UDI. The recordkeeping, reporting, and third-party disclosure requirements referenced in the notice are imposed on any person who causes a label to be applied to a device, or who causes the label to be modified, with the intent that the device will be commercially distributed without any subsequent replacement or modification of the label. To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2019-07-31/pdf/2019-16269.pdf?ref=fdaweb.com).