Link to episode on Apple Podcasts
A summary of two FDA webinars discussing Unique Device Identifiers (UDI) and Global Unique Device Identifier Database (GUDID). Learn what information is incorporated into UDIs and what devices are affected by UDI and GUDID registration.
References:
Workshops & Conferences (Medical Devices) > Webinars: UDI 101 and Getting Ready for GUDID – January 14, 2015 (archive-it.org)
UDI IMPLEMENTATION ROADMAP (fda.gov)
UDI Rule and Guidances, Training, Resources, and Dockets | FDA
Bonus Episode 2 – FDA Standards for Unique Device Identifiers and Upcoming Compliance Dates