BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PHOTOFACIAL, SCITON BBL

    MDR report key: 1031650 · Received April 16, 2008

    Report

    Report Number
    MW5006326
    Event Type
    Injury
    Date Received
    April 16, 2008
    Date of Event
    November 20, 2007
    Report Date
    April 16, 2008
    Manufacturer
    SCITON
    Product Code
    GEX
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NC, US
    Reporter Occupation
    PATIENT

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PHOTOFACIAL, SCITON BBL SCITON BBL GEX SCITON

    Patients

    Seq Age Sex Outcome Treatment
    1 38 YR Other