BEUDAMED
    FDA Adverse Event Other Summary report: N

    1213649-2000-00001

    MDR report key: 285520 · Received June 16, 2000

    Report

    Report Number
    1213649-2000-00001
    Event Type
    Other
    Date Received
    June 16, 2000
    Date of Event
    May 25, 2000
    Product Code
    DWO
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DWO

    Patients

    Seq Age Sex Outcome Treatment
    1