BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TUMT & PROSTATRON

    MDR report key: 311131 · Received December 28, 2000

    Report

    Report Number
    MW1020756
    Event Type
    Injury
    Date Received
    December 28, 2000
    Date of Event
    June 15, 2000
    Report Date
    December 28, 2000
    Manufacturer
    EDAP TECHNOMED, INC.
    Product Code
    MEQ
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    PATIENT

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TUMT & PROSTATRON MICROWAVE THERAPY MEQ EDAP TECHNOMED, INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 65 YR Hospitalization