Medical Devices

GUDID Web Interface

Device labelers may submit, search and retrieve information about their devices via the GUDID Web Interface, which enables structured input of information one DI record at a time.

To submit device information via the GUDID Web Interface, labelers must first obtain a GUDID account.

To assist labelers in submitting data to the GUDID, the FDA has created a GUDID User Manual. This document contains step-by-step technical instructions for submitting data via the GUDID web interface, including screenshots. The FDA intends to periodically update this document to reflect system changes and enhancements.

Launch GUDID Web Interface

The public can search and download information from the GUDID at AccessGUDID.

Page Last Updated: 05/04/2015
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