BEUDAMED
    FDA Adverse Event Other Summary report: N

    6000032-2000-00351

    MDR report key: 308509 · Received December 6, 2000

    Report

    Report Number
    6000032-2000-00351
    Event Type
    Other
    Date Received
    December 6, 2000
    Date of Event
    August 21, 2000
    Product Code
    LGW
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1