BEUDAMED
    FDA Adverse Event Other Summary report: N

    1213649-2001-00002

    MDR report key: 369676 · Received December 20, 2001

    Report

    Report Number
    1213649-2001-00002
    Event Type
    Other
    Date Received
    December 20, 2001
    Date of Event
    December 11, 2001
    Product Code
    KNW
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    57946 KNW

    Patients

    Seq Age Sex Outcome Treatment
    1