BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SUREFIRE SCORPION NEEDLE

    MDR report key: 1970599 · Received November 30, 2010

    Report

    Report Number
    1970599
    Event Type
    Malfunction
    Date Received
    November 30, 2010
    Date of Event
    November 5, 2010
    Report Date
    November 30, 2010
    Manufacturer
    ARTHREX, INC.
    Product Code
    GAT
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MI, US

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SUREFIRE SCORPION NEEDLE SUTURE, NEEDLE GAT ARTHREX, INC. AR-13991N 342682

    Patients

    Seq Age Sex Outcome Treatment
    1 51 YR