BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    M SERIES

    MDR report key: 287704 · Received July 28, 2000

    Report

    Report Number
    1220908-2000-00741
    Event Type
    Malfunction
    Date Received
    July 28, 2000
    Report Date
    July 1, 2000
    Manufacturer
    ZOLL MEDICAL CORP.
    Product Code
    KRF
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    HK
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    COMPLAINANT ALLEGED THAT DURING BIOMEDICAL TESTING AND ROUTINE PREVENTIVE MAINTENANCE OF THE DEVICE, THERE WAS NO VIDEO DISPLAY WHEN THE DEVICE WAS POWERED ON. THE COMPLAINANT INDICATED THAT THERE WAS NO PT INVOLVEMENT IN THE REPORTED MALFUNCTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 M SERIES DEFIBRILLATOR/PACEMAKER KRF ZOLL MEDICAL CORP. MSERIES NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other