BEUDAMED
    FDA Adverse Event Death Summary report: N

    VIRIDIA INFORMATION CENTER

    MDR report key: 284736 · Received July 5, 2000

    Report

    Report Number
    1218950-2000-00025
    Event Type
    Death
    Date Received
    July 5, 2000
    Date of Event
    May 29, 2000
    Report Date
    May 31, 2000
    Manufacturer
    AGILENT TECHNOLOGIES, INC.
    Product Code
    DRT
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED TO AGILENT TECHNOLOGIES THAT WHEN THE PT WENT INTO VENTRICULAR FIBRILLATION, THERE WAS NO AUDIBLE ALARM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VIRIDIA INFORMATION CENTER ARRHYTHMIA DRT AGILENT TECHNOLOGIES, INC. M3150A NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Death