BEUDAMED
    FDA Adverse Event Other Summary report: N

    RADIAL ARTERY CATHETERIZATION SET

    MDR report key: 31650 · Received April 1, 1996

    Report

    Report Number
    MW1008773
    Event Type
    Other
    Date Received
    April 1, 1996
    Date of Event
    March 7, 1996
    Report Date
    March 12, 1996
    Manufacturer
    ARROW INTL, INC.
    Product Code
    DXE
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    THE ENCLOSED LETTER REFERENCING MW1008773 WAS SENT TO CO'S ATTENTION FOR INFO REGARDING A MEDWATCH REPORT. CO FORWARDED THE LETTER ON TO THE MFR, ARROW INTL, INC.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RADIAL ARTERY CATHETERIZATION SET RADIAL ARTERY CATHETERIZATION SET DXE ARROW INTL, INC. RA 04020 203245

    Patients

    Seq Age Sex Outcome Treatment
    1 69 YR Other