BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BUCKY DIAGNOST CS 2

    MDR report key: 301588 · Received October 18, 2000

    Report

    Report Number
    1217116-2000-00019
    Event Type
    Malfunction
    Date Received
    October 18, 2000
    Date of Event
    September 26, 2000
    Report Date
    October 9, 2000
    Manufacturer
    PHILIPS SYSTEME MEDEZIN
    Product Code
    IYB
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OK, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    REPORTEDLY, AS THE CS X-RAY TUBE CEILING SUSPENSION WAS BEING MOVED INTO A LATCHED POSITION, THE FRONT COVER DETACHED FROM THE CEILING SUSPENSION AND FELL ON A RADIOLOGY/X-RAY STUDENT. REPORTEDLY, THE STUDENT WAS NOT INJURED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BUCKY DIAGNOST CS 2 DIAGNOSTIC X-RAY TUBE MOUNT IYB PHILIPS SYSTEME MEDEZIN 9890-010-06521 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN