BEUDAMED
    FDA Adverse Event Other Summary report: N

    PATHFINDER MINI

    MDR report key: 310866 · Received December 28, 2000

    Report

    Report Number
    2951009-2000-00005
    Event Type
    Other
    Date Received
    December 28, 2000
    Date of Event
    January 11, 1999
    Report Date
    December 22, 2000
    Manufacturer
    CARDIMA, INC.
    Product Code
    DRF
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    PHYSICIAN

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PATHFINDER MINI MAPPING CATHETER DRF CARDIMA, INC. NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 53 YR Other NO INFO.