BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DEFIBRILLATOR/MONITOR/PACEMAKER

    MDR report key: 14139 · Received June 17, 1994

    Report

    Report Number
    MW1002498
    Event Type
    Injury
    Date Received
    June 17, 1994
    Date of Event
    June 9, 1994
    Report Date
    June 14, 1994
    Manufacturer
    ZOLL MEDICAL CORP.
    Product Code
    LDD
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    UT, US
    Reporter Occupation
    BIOMEDICAL ENGINEER

    Narratives

    Description of Event or Problem · 1

    SYNCHRONIZED CARDIOVERSION WILL NOT WORK ON V-TACH SIGNALS PROVIDED BY ANOTHER CO'S SIMULATOR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DEFIBRILLATOR/MONITOR/PACEMAKER DEFIBRILLATOR/MONITOR/PACEMAKER LDD ZOLL MEDICAL CORP. PD-1200

    Patients

    Seq Age Sex Outcome Treatment
    1 * Life Threatening DYNATECH MEDTESTER 5000