BEUDAMED
    FDA Adverse Event Injury Summary report: N

    QUINTON PERMCATH INSERTION KIT

    MDR report key: 108011 · Received July 23, 1997

    Report

    Report Number
    3014398-1997-00074
    Event Type
    Injury
    Date Received
    July 23, 1997
    Date of Event
    June 10, 1997
    Manufacturer
    QUINTON INSTRUMENT CO
    Product Code
    LFK
    Report Source
    Manufacturer report

    Narratives

    Description of Event or Problem · 1

    (IN SUBSEQUENT FOLLOW-UP WITH THE RPTR IT WAS CLARIFIED THAT THE SHEATH SEGMENT WAS APPROX 2 X.3 CM AND WAS MANIPULATED INTO THE RIGHT FEMORAL VEIN BY MEANS OF A SNARE.)

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 QUINTON PERMCATH INSERTION KIT HEMODIALYSIS CATHETER LFK QUINTON INSTRUMENT CO NA 800789-1997-03

    Patients

    Seq Age Sex Outcome Treatment
    1 *