BEUDAMED
    FDA Adverse Event Death Summary report: N

    SIEMENS

    MDR report key: 189777 · Received September 29, 1998

    Report

    Report Number
    MW1014655
    Event Type
    Death
    Date Received
    September 29, 1998
    Date of Event
    August 27, 1998
    Report Date
    September 10, 1998
    Manufacturer
    SIEMENS MEDICAL SYSTEMS, INC. ELECTRO MEDICAL DIVISON
    Product Code
    DRT
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    PT HAD CARDIAC ARREST. THE CARDIAC MONITOR ALARMS WERE NOT ACTIVATED. PT WAS ON A TELEMETRY PACK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SIEMENS CARDIAC MONITOR DRT SIEMENS MEDICAL SYSTEMS, INC. ELECTRO MEDICAL DIVISON CPD - 155F1 *
    2 UNK TELEMETRY TRANSMITTER PACK DRG SIEMENS MEDICAL SYSTEMS, INC. ELECTROMEDICAL DIVISION 3371098 E510U *

    Patients

    Seq Age Sex Outcome Treatment
    1 66 YR Death