BEUDAMED
    FDA Adverse Event Other Summary report: N

    ALL TOSHIBA CT SCANNERS

    MDR report key: 1083461 · Received July 28, 2008

    Report

    Report Number
    MW5007817
    Event Type
    Other
    Date Received
    July 28, 2008
    Report Date
    July 28, 2008
    Manufacturer
    TOSHIBA
    Product Code
    JAK
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    FAILURE TO PROVIDE AIAT INFORMATION "UPON REQUEST".

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ALL TOSHIBA CT SCANNERS ALL CT SCANNERS JAK TOSHIBA

    Patients

    Seq Age Sex Outcome Treatment
    1 ALL CT SCANNERS MANUFACTURED BY TOSHIBA