BEUDAMED
    FDA Adverse Event Summary report: N

    LIGAMAX

    MDR report key: 3200856 · Received June 26, 2013

    Report

    Report Number
    3200856
    Date Received
    June 26, 2013
    Date of Event
    June 20, 2013
    Report Date
    June 25, 2013
    Manufacturer
    ETHICON ENDO SURGERY
    Product Code
    FZP
    Report Source
    User Facility report
    Reporter Location
    MI, US

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    291393 LIGAMAX SURGICAL STAPLER FZP ETHICON ENDO SURGERY * J4CL2J

    Patients

    Seq Age Sex Outcome Treatment
    1 65 YR