BEUDAMED
    FDA Adverse Event Summary report: N

    ALARIS TRI-SITE

    MDR report key: 3200855 · Received June 7, 2013

    Report

    Report Number
    3200855
    Date Received
    June 7, 2013
    Date of Event
    June 3, 2013
    Report Date
    June 7, 2013
    Manufacturer
    CAREFUSION
    Product Code
    FLL
    Report Source
    User Facility report
    Reporter Location
    CA, US
    Reporter Occupation
    RISK MANAGER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    253988 ALARIS TRI-SITE THERMOMETER FLL CAREFUSION * *

    Patients

    Seq Age Sex Outcome Treatment
    1 26 YR