BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BIOPINCE

    MDR report key: 676501 · Received February 9, 2006

    Report

    Report Number
    1036710-2006-00001
    Event Type
    Malfunction
    Date Received
    February 9, 2006
    Date of Event
    January 7, 2006
    Report Date
    February 7, 2006
    Manufacturer
    MEDICAL DEVICE TECHNOLOGIES, INC.
    Product Code
    KNW
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    UNIT MALFUNCTIONED AND PIERCED PHYSICIAN'S THUMBNAIL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BIOPINCE SOFT TISSUE BIOPSY DEVICE KNW MEDICAL DEVICE TECHNOLOGIES, INC. * 53932

    Patients

    Seq Age Sex Outcome Treatment
    1 * Required Intervention