BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 518600 · Received January 28, 2004

    Report

    Report Number
    9680515-2003-00004
    Event Type
    Other
    Date Received
    January 28, 2004
    Date of Event
    October 21, 2003
    Manufacturer
    *
    Product Code
    KNS
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 *