BEUDAMED
    FDA Adverse Event Death Summary report: N

    AGILENT INFORMATION CENTER

    MDR report key: 371043 · Received January 11, 2002

    Report

    Report Number
    1218950-2002-00007
    Event Type
    Death
    Date Received
    January 11, 2002
    Date of Event
    January 1, 2002
    Report Date
    January 3, 2002
    Manufacturer
    AGILENT TECHNOLOGIES, INC.
    Product Code
    DRT
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE MONITORING SYSTEM DID NOT ALARM WHEN THE PATIENT WENT INTO A BRADY CONDITION.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Death