BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SUCTION CATHETER

    MDR report key: 33043 · Received May 13, 1996

    Report

    Report Number
    MW4001197
    Event Type
    Malfunction
    Date Received
    May 13, 1996
    Report Date
    February 9, 1995
    Manufacturer
    MEDOVATIONS, INC.
    Product Code
    KDH
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    DC, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THIS ITEM DOES NOT HAVE THE PROPER MEASUREMENTS TO GUIDE PLACEMENT FOR SUCTIONING. 6FR FEEDING TUBE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SUCTION CATHETER SUCTION CATHETER KDH MEDOVATIONS, INC. D1100-06 580187

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO