UDI and MU3: What Data Goes in the Item Master?
Susan Morris, CMRP, FAHRMM, health care executive, Cerner Corporation, explains the different parts of the Unique Device Identifier (UDI) and which part should go into the Item Master.
This webcast walks through the three FDA-accredited issuing agencies that assign UDIs and explains what information is in the different barcodes and how to read them both electronically and by human sight.
Related Resources
Advisory
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
Letter/Comment
Recent Guidance on Meaningful Use of EHRs Makes Compliance More Difficult.
Request for Proposals (RFP)
Medical Surgical Supply Distribution Request for Proposal.
Issue Brief
This learning lab covers alarm safety management in the health care supply chain field.
Request for Proposals (RFP)
A sample of a CT scanner RFP covering all the basics. Download the document and tailor it to your needs.
Letter/Comment
This page provides information about submitting data to the database for device Labelers, entities responsible for providing the data to the GUDID.