Global Unique Device Identification Database (GUDID) Draft Guidance for Industry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

Magazine & Journal Articles
Navigating the Economic Storm: A Prescriptive Approach for Healthcare Supply Chain Professionals
In this page, AHRMM recommends these 3 proactive activities in the event of economic downturn.
Guides and Reports
University of Houston Hospital Supply Chain Study Results
In the fall of 2014, the University of Houston conducted a national study on hospital supply chain.
Advisory
Final Regulations on Taxable Medical Devices
The final regulations that provide guidance on the excise tax imposed on the sale of certain medical devices, enacted by the Health Care and Educ
Advisory
Interim Guidance for Infection Control for Care of Patients with Confirmed or Suspected Swine Influenza A (H1N1) Virus Infection in a Healthcare Setting
This document provides interim guidance for infection control for healthcare facilities (e.g., hospitals, long-term care and outpatient facilities,…
On-Demand Educational Webinars
Service Contracts: Impacting the Total Cost of Ownership