BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MIDAS REX I MO

    MDR report key: 321216 · Received February 28, 2001

    Report

    Report Number
    1625507-2001-00488
    Event Type
    Malfunction
    Date Received
    February 28, 2001
    Report Date
    October 15, 1999
    Manufacturer
    MEDTRONIC MIDAS REX
    Product Code
    HBB
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    EXCESSIVE VIBRATING WHEN SLEEVE IS ATTACHED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    8129 MIDAS REX I MO PNEUMATIC SURGICAL DRILL HBB MEDTRONIC MIDAS REX NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 *