BEUDAMED
    FDA Adverse Event Other Summary report: N

    ZOLL MEDICAL CORPORATION

    MDR report key: 829867 · Received March 16, 2007

    Report

    Report Number
    MW1042263
    Event Type
    Other
    Date Received
    March 16, 2007
    Date of Event
    December 26, 2006
    Report Date
    March 5, 2007
    Manufacturer
    *
    Product Code
    MKJ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    VERIFIED THAT UNIT WILL NOT POWER UP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ZOLL MEDICAL CORPORATION DEFIBRILLATOR, MONITOR, PACEMAKER MKJ * M SERIES NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other