BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SILIMED

    MDR report key: 1060690 · Received June 10, 2008

    Report

    Report Number
    MW5007298
    Event Type
    Injury
    Date Received
    June 10, 2008
    Date of Event
    March 7, 2008
    Report Date
    June 10, 2008
    Manufacturer
    *
    Product Code
    FWM
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NV, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    REMOVAL OF BILATERAL BREAST IMPLANTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SILIMED BREAST IMPLANTS FWM * * *

    Patients

    Seq Age Sex Outcome Treatment
    1 35 YR