BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ICON

    MDR report key: 215580 · Received March 16, 1999

    Report

    Report Number
    1423253-1999-00001
    Event Type
    Malfunction
    Date Received
    March 16, 1999
    Date of Event
    February 1, 1999
    Report Date
    February 16, 1999
    Manufacturer
    SIEMENS MEDICAL SYSTEMS, INC. NMG GROUP
    Product Code
    JWM
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    INCONSISTENT RESULTS MAY OCCUR WHILE SAVING DATA TWICE ON THE PROCESSING PAGE IN THE AUTOPERFUSION PROGRAM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ICON COMPUTER JWM SIEMENS MEDICAL SYSTEMS, INC. NMG GROUP NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other