BEUDAMED
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    TFT ELECTRONICS LTD

    FDA registration
    TFT ELECTRONICS LTD·1 product·🇬🇧 United Kingdom

    GE Vivid E9 ultrasound system. GE Vivid E9 is a Track 3 diagnostic ultrasound system, which is primarily intended for cardiac imaging and analysis, but which also includes vascular and general radiology applications. The Vivid E9 incorporates a variety of electronic array transducers operating in linear, curved linear, sector/phased array or matrix array format, including two dedicated CW transducers and several real time 3D transducers. It consists of a mobile console with keyboard control panel; color LCD/TFT touch panel, LCD color video display and optional image storage and printing devices. It provides high performance ultrasound imaging and analysis and has comprehensive networking and DICOM capability.

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code IYO·October 11, 2013

    GE Vivid E9 ultrasound system. GE Vivid E9 is a Track 3 diagnostic ultrasound system, which is primarily intended for cardiac imaging and analysis, but which also includes vascular and general radiology applications. The Vivid E9 incorporates a variety of electronic array transducers operating in linear, curved linear, sector/phased array or matrix array format, including two dedicated CW transducers and several real time 3D transducers. It consists of a mobile console with keyboard control panel; color LCD/TFT touch panel, LCD color video display and optional image storage and printing devices. It provides high performance ultrasound imaging and analysis and has comprehensive networking and DICOM capability.

    FDA Enforcement
    Class II ·Terminated·GE Healthcare, LLC·November 27, 2013

    TT ELECTRONICS

    FDA registration
    TT ELECTRONICS·1 product·🇺🇸 United States

    KWONG KEI TAT ELECTRONIC TECHNOLOGY (VIETNAM) CO., LTD

    FDA registration
    KWONG KEI TAT ELECTRONIC TECHNOLOGY (VIETNAM) CO., LTD·1 product·🇻🇳 Vietnam

    TELECTRONIC

    FDA Adverse Event
    Injury ·TELECTRONICS·Product code DTB·July 3, 1997

    MARATHON DR

    FDA Adverse Event
    Malfunction ·SULZER INTERMEDICS INC.·Product code DXY·July 10, 1997

    Extron Electronics OEM, CAB, DVI-I to DVI (3ft.); Part #: 43-112-01 (Stryker Part #: 0100-224-108); Distributed by Stryker Communications, Flower Mound, TX 75028. (These cables are commonly used with the Switchpoint Infinity II)

    FDA Recall
    Terminated ·Stryker Communications·Product code GCJ·October 3, 2007

    META DDDR 1254

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIV.·Product code DXY·October 9, 1997

    HITACHI

    FDA Adverse Event
    Injury ·*·Product code LNH·January 11, 2002

    LG Electronics Magyar Kft.

    Importer
    🇭🇺 Hungary

    PRIM, S.A.

    Importer
    🇪🇸 Spain·64 Manufacturers

    MedPath GmbH

    Authorized representative
    🇩🇪 Germany·537 Manufacturers·13464 Devices

    SUNGO Europe B.V.

    Authorized representative
    🇳🇱 Netherlands·1571 Manufacturers·20390 Devices