BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    CALI-LOOP

    FDA 510(k)
    FDA Class 1 ·Microbiology

    PressON™

    FDA UDI
    NEXUS SPINE, L.L.C.·B6788203450·Wand – Outer, 70mm

    ARTHREX UNIVERS FRACTURE PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HONOUR SPACER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·May 9, 2014

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·November 6, 2012

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code MDS·August 30, 2010

    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