BEUDAMED
    FDA Adverse Event Other Summary report: N

    1221842-1998-00002

    MDR report key: 178182 · Received July 17, 1998

    Report

    Report Number
    1221842-1998-00002
    Event Type
    Other
    Date Received
    July 17, 1998
    Date of Event
    June 26, 1998
    Product Code
    LZS
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1