BEUDAMED
    FDA Adverse Event Other Summary report: N

    ARROW INTERNATIONAL

    MDR report key: 597481 · Received April 25, 2005

    Report

    Report Number
    597481
    Event Type
    Other
    Date Received
    April 25, 2005
    Date of Event
    April 20, 2005
    Report Date
    April 25, 2005
    Manufacturer
    ARROW INTERNATIONAL, INC.
    Product Code
    DQO
    Report Source
    User Facility report
    Reporter Location
    NM, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    THE GUIDE WIRE WAS OUTSIDE THE CATHETER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ARROW INTERNATIONAL RADIAL ARTERY CATHETERIZATION SET (22GA) DQO ARROW INTERNATIONAL, INC. * 0B0137

    Patients

    Seq Age Sex Outcome Treatment
    1 71 YR Other