BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 503624 · Received December 4, 2003

    Report

    Report Number
    9610617-2003-00029
    Event Type
    Other
    Date Received
    December 4, 2003
    Date of Event
    November 17, 2003
    Manufacturer
    *
    Product Code
    FFK
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 *