Unique Device Identifier (UDI)
An announcement of GUDID Release 2.2 deployment and document updates.
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…
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WORK GROUP TITLE:UDI Capture Work GroupCASE STUDY PARTICIPANTS:Sandi Michel, MPMP, ITIL, CLSSBB, Director of Supply Chain Systems and Quality, the Office of Data Standards & Interoperability for Franciscan Missionaries of Our Lady Health System (FMOLHS)CASE STUDY ORGANIZATION:
CASE STUDY PARTICIPANTS:
Lawrence Gossman, AVP, Supply Chain, Fran Sercer, MSN RN, Associate Director of Interventional Services, Anita Sears, Director of Supply Chain, Eskenazi Health
In an effort to better protect patients during product recalls, and to improve care at a population health level, hospitals must begin to accurately capture medical device data through UDI adoption.
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This paper will define the regulation and explore how a supply chain department can support their organization in meeting this aspect of the regulations. Understanding the alphabet soup of acronyms that is Unique Device Identifier (UDI), their meaning, how to understand and read the standardized…
A UDI Capture Work Group Case Study at the Baptist Health.