BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    MICROLASE 8 0 0 (OPHTHALMIC LASER)

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690127284·Apex Revision Knee System-Common Instruments Pan

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690195009·Apex Revision Knee System-Common Instruments Pa...

    NEEDLE, TRUCARE VACUTAINER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Cepheid Xpert Respiratory Control Panel

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ECHELON LINEAR CUTTER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 24, 2014

    THERAPEUTIC PLASMA EXCHANGE SET

    FDA Adverse Event
    Injury ·CARIDIANBCT·Product code LKN·October 28, 2010

    DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·December 28, 2012

    Stryker T2 Arthrodesis Nailing System. Manufacturer: Stryker Trauma GmbH, Professor-Kuntscher-Str. 1-5, 24232 Schonkirchen Germany. Distributed in the USA by Stryker Orthopaedics, 325 Corporate Drive, Mahwah, NJ 07430. The T2 Arthrodesis Nail is intended for the treatment of Knee Arthrodesis. The design of the T2 Arthrodesis Nail features a unique curvature which incorporates both femur ante curvature and knee valgus bend. Indications: Aseptic failed total knee arthro-plasty with or without bone loss; Failed external fixation, non unions and malunions; Periarticular fractures where repair is not possible; Pathologic fractures and tumor resections; Pseudoarthrosis and correct osteotomy; Ipsilateral femur fractures; and Open and closed femoral fractures.

    FDA Enforcement
    Class II ·Terminated·Stryker Howmedica Osteonics Corp.·July 25, 2012

    OEC 9800; OEC FluoroTrak 9800 Plus; OEC 9800 Plus; OEC 9800 MD Motorized C-arm System, 892.1650 Image-intensified fluoroscopic x-ray system. The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. The system includes features specifically designed for use in diagnostic and interventional cardiac imaging procedures and is also intended for cholangiography, endoscopic, urologic orthopedic, neurologic, vascular, critical care and emergency room procedures. It may be used for other imaging applications at the physician's discretion.

    FDA Enforcement
    Class I ·Terminated·GE OEC Medical Systems, Inc·August 1, 2012