Global Unique Device Identification Database (GUDID) Draft Guidance for Industry

By Center for Devices and Radiological Health, Informatics Staff, U.S. Department of Health and Human Services Food and Drug Administration, AHRMM
This document is intended to provide information about submitting data to the database for device Labelers, entities responsible for providing the data to the GUDID.
 

Related Resources

On-Demand Educational Webinars
Help! I Can’t Find My OR Supplies!
Tracking surgical supplies is a challenge. Average returns for picked supplies is low, O.R. in-and-out traffic to retrieve items is high, and…
On-Demand Educational Webinars
Product Disruptions Are Impacting My Business Continuity
Business continuity ensures that an organization can continue to operate in the event of a serious incident or disaster and encompasses strategic…
On-Demand Educational Webinars
Annual Clinical Contract Evaluations: Are You Ready?
In this webinar, we discuss the clinical contract evaluation process, including government requirements, expectations, and improving contract…
On-Demand Educational Webinars
From First Curve to Second: Hospital and Care Systems of the Future
Through its Hospitals in Pursuit of Excellence (HPOE) strategic platform, the American Hospital Association (AHA) has studied the role of the…
On-Demand Educational Webinars
Hospital Collaboration Pays Off Even for Implants
Yankee Alliance facilitated an Orthopedic Total Joint Collaborative in order to identify opportunities for quality improvement and cost reduction,…
On-Demand Educational Webinars
Now's the Time! We Must Engage Physicians to Reduce Costs and Improve Outcomes
This AHRMM webinar will help engage physicians to reduce costs and improve patient outcomes.