BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DIAGNOST 76 PLUS

    MDR report key: 121152 · Received September 15, 1997

    Report

    Report Number
    1217116-1997-00030
    Event Type
    Malfunction
    Date Received
    September 15, 1997
    Date of Event
    August 3, 1997
    Report Date
    August 16, 1997
    Manufacturer
    PHILIPS SYSTEME MEDEZIN
    Product Code
    IXQ
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    REPORTEDLY, WHEN THE TECHNOLOGIST MOVED THE TABLETOP IN THE LONGITUDINAL DIRECTION, THE PT'S FINGERS ALLEGEDLY GOT CAUGHT UNDER THE TABLETOP PINCHING THEM AGAINST THE TABLE. NO SERIOUS INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DIAGNOST 76 PLUS GENERAL PURPOSE R/F SYSTEM IXQ PHILIPS SYSTEME MEDEZIN NI NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other