BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    Cocoon Convective Warming System, Model CWS7000

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VARIAX 2 SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Resonic Rapid Acoustic Pulse Device

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    GE OEC 9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·November 13, 2008

    CANE, CRUTCH AND WALKER TIPS AND PADS

    FDA Adverse Event
    KENSTONE METAL·Product code INP·September 2, 2011

    ORTHO SUMMIT SAMPLE HANDLING SYSTEM

    FDA Adverse Event
    Malfunction ·HAMILTON BONADUZ AG·Product code MMH·July 18, 2013

    Allura Exper FD Series. System codes 722003 722010 722022 722005 722011 722019 722001 722002 722006 722012 722008 722013 722020 722025 722015 722023 722038 889006 889016 889009 722005 The device is an X-Ray Generator.

    FDA Enforcement
    Class II ·Terminated·Philips North America, LLC·March 25, 2020