BEUDAMED
    FDA Adverse Event Other Summary report: N

    GOODTECH THERMODILUTION CATHETER, PVC

    MDR report key: 653740 · Received December 15, 2005

    Report

    Report Number
    2243801-2005-00009
    Event Type
    Other
    Date Received
    December 15, 2005
    Date of Event
    March 3, 2004
    Report Date
    December 7, 2005
    Manufacturer
    B. BRAUN MEDICAL, INC.
    Product Code
    DYG
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    CUT DAB (DISTAL ARTERIAL BALLOON).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GOODTECH THERMODILUTION CATHETER, PVC THERMODILUTION CATHETER DYG B. BRAUN MEDICAL, INC. NA 60483852

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other