BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BARDEX

    MDR report key: 3201009 · Received June 10, 2013

    Report

    Report Number
    3201009
    Event Type
    Malfunction
    Date Received
    June 10, 2013
    Date of Event
    May 6, 2013
    Report Date
    June 10, 2013
    Manufacturer
    CR BARD
    Product Code
    KOD
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    ID, US

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    262160 BARDEX CATHETER KOD CR BARD * JW1161

    Patients

    Seq Age Sex Outcome Treatment
    1 *