BEUDAMED
    FDA Adverse Event Death Summary report: N

    VIRIDIA INFORMATION CENTER

    MDR report key: 273796 · Received April 12, 2000

    Report

    Report Number
    1218950-2000-00014
    Event Type
    Death
    Date Received
    April 12, 2000
    Date of Event
    March 10, 2000
    Report Date
    March 13, 2000
    Manufacturer
    AGILENT TECHNOLOGIES, INC.
    Product Code
    DRT
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED TO AGILENT TECHNOLOGIES THAT THE PT WAS FOUND UNRESPONSIVE. NO ALARM SOUNDED. A CODE WAS CALLED AND RESUSCITATION WAS UNSUCCESSFUL.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Death