BEUDAMED
    FDA Adverse Event Other Summary report: N

    BARD URETHERAL CATHETER

    MDR report key: 548056 · Received December 31, 2003

    Report

    Report Number
    548056
    Event Type
    Other
    Date Received
    December 31, 2003
    Date of Event
    November 22, 2003
    Report Date
    December 31, 2003
    Manufacturer
    C.R. BARD, INC.
    Product Code
    FAD
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    DC, US
    Reporter Occupation
    RISK MANAGER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BARD URETHERAL CATHETER 6 FRENCH WHISTLE TIP URETHERAL STENT CATHETER FAD C.R. BARD, INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 15 YR