BEUDAMED
    FDA Adverse Event Summary report: N

    CLINSTAR LABORATORY COMPUTER SYSTEM

    MDR report key: 26010 · Received September 26, 1995

    Report

    Report Number
    MW1007016
    Date Received
    September 26, 1995
    Report Date
    September 20, 1995
    Manufacturer
    HBO & CO.
    Product Code
    LNX
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    MEDICAL TECHNOLOGIST

    Narratives

    Description of Event or Problem · 1

    PT REPORTS PRINTING OUT WITHOUT COMMENTS ENTERED BY TECHNOLOGISTS THAT WOULD AFFECT INTERPRETATION OF THE TESTS. THIS ONLY OCCURS WITH RESULTS PRINTED TO REMOTE SITES VIA TELEPHONE MODEMS. REPORTS PRINTED ON-SITE OR DISPLAYED ON COMPUTER TERMINALS HAVE COMPLETE RESULT COMMENTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CLINSTAR LABORATORY COMPUTER SYSTEM COMPUTER SYSTEM LNX HBO & CO.

    Patients

    Seq Age Sex Outcome Treatment
    1 *