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
Webcast
An update on current FDA and Congressional activity on independent service for reusable medical devices and the potential impact on your costs and
Case Studies
A UDI Capture Work Group Case Study at the Baptist Health.
Webcast
In part one, we explore the reasons why the FDA created the (UOU) Unit of Use.