BEUDAMED
    FDA Adverse Event Other Summary report: N

    BARDEX

    MDR report key: 286829 · Received July 20, 2000

    Report

    Report Number
    MW1019338
    Event Type
    Other
    Date Received
    July 20, 2000
    Date of Event
    May 25, 2000
    Report Date
    July 17, 2000
    Manufacturer
    C.R. BARD, INC.
    Product Code
    KOD
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    8 FR CATHETER UNABLE TO BLEED THROUGH (PRIME). NO PT INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BARDEX FOLEY CATHETER 8 FR 3CC KOD C.R. BARD, INC. NA KY945

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other