---
kind: "section"
citation: "21 C.F.R. § 830.340"
title: "21"
number: "830.340"
heading: "Voluntary submission of ancillary device identification information."
url: "https://uscodex.org/cfr/21/830.340"
---

# §830.340. Voluntary submission of ancillary device identification information.

- (a) You may not submit any information to the Global Unique Device Identification Database (GUDID) other than that specified by [§ 830.310](/cfr/21/830.310.md), except where FDA acts to permit the submission of specified additional types of information, termed ancillary information.
- (b) FDA will provide information through the FDA Web site at http://www.fda.gov/udi/ concerning the types of ancillary information that may be submitted to the GUDID.
- (c) FDA may periodically change the types of ancillary information that may be submitted to the GUDID. We will announce any change on the FDA Web site at http://www.fda.gov/udi/ at least 60 days before making the change.

## Notes

### Source

Source: 78 FR 58826, Sept. 24, 2013, unless otherwise noted.

### Authority

Authority: 21 U.S.C. 321, 331, 352, 353, 360, 360d, 360i, 360j, 371.

### Source

Source: 78 FR 58823, Sept. 24, 2013, unless otherwise noted.