BEUDAMED
    FDA Adverse Event Injury Summary report: N

    *

    MDR report key: 509283 · Received February 2, 2004

    Report

    Report Number
    9614385-2003-00204
    Event Type
    Injury
    Date Received
    February 2, 2004
    Date of Event
    November 19, 2003
    Manufacturer
    *
    Product Code
    FWM
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 *