BEUDAMED
    FDA Adverse Event Other Summary report: N

    GE MEDICAL

    MDR report key: 746531 · Received September 21, 2005

    Report

    Report Number
    MW1036680
    Event Type
    Other
    Date Received
    September 21, 2005
    Date of Event
    August 19, 2005
    Report Date
    August 23, 2005
    Manufacturer
    GE MEDICAL
    Product Code
    DXK
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    GA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    TEE ECHO STUDY DONE AND TRANSMITTED FROM MACHINE. LOST FROM HARD DRIVE INCLUDING ALL ALPHA AND NUMERICAL DATA.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GE MEDICAL VIVID 7 ECHO PAC DXK GE MEDICAL GE VIVID 7 BT 02 PLUS

    Patients

    Seq Age Sex Outcome Treatment
    1 49 YR Other