PORTFOLIO


FMOL Health System UDI Capture Work Group Case Study


CLIENT

Association for Healthcare Resource & Materials Management (AHRMM)

CATEGORY

Recent Client Work

ABOUT PROJECT

FMOLHS is now working to use the device identifier (DI) portion of the UDI for product identification at the point of use in the operating room (OR), alongside the U.S. Food and Drug Administration’s (FDA) unique device identification (UDI) rule. FMOLHS is requesting supplier DIs for all products coming into the organization, adding them to its Lawson enterprise resource planning (ERP) system, which feeds this standardized product data to a third party UDI tracking solution. FMOLHS is also exploring alternatives, including accessing DIs from suppliers through the Global Unique Device Identification Database (GUDID).


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