BEUDAMED
    FDA Adverse Event Injury Summary report: N

    45MM ARTICNG LNR CUTR LONG

    MDR report key: 663200 · Received January 6, 2006

    Report

    Report Number
    1527736-2006-00086
    Event Type
    Injury
    Date Received
    January 6, 2006
    Date of Event
    December 21, 2005
    Report Date
    January 4, 2006
    Manufacturer
    ETICON ENDO SURGERY, INC
    Product Code
    KOG
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 45MM ARTICNG LNR CUTR LONG ENDO LINEAR CUTTERS-ETS45MM KOG ETICON ENDO SURGERY, INC NA A4C13C

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention