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

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    CORDIS RIGHT-ANGLE CATHETER GUIDE

    FDA 510(k)
    FDA Class 2 ·Neurology

    IMMUNO-TROL LOW CELLS

    FDA 510(k)
    FDA Class 2 ·Hematology

    CATHETER CONNECTIONS' DUALCAP SOLO

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CORE UNIVERSAL DRIVER

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code HBE·November 26, 2010

    MEGA SUTURECUT NEEDLE DRIVER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 3, 2014

    LIGASURE ATLAS HANDSWITCHING 37CM

    FDA Adverse Event
    Malfunction ·COVIDIEN LLC (SHANGHAI)·Product code GEI·December 5, 2012

    PM3544 QUADRA RELIEVE and PM3562 QUADRA ALLURE MP These low voltage (LV) devices are implantable pacemaker pulse generators, intended to be permanently implanted in the body, that have a power supply and electronic circuits that produce a periodic electrical pulse to stimulate the heart. These devices are used as a substitute for the heart's intrinsic pacing system to correct both intermittent and continuous cardiac rhythm disorders

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·October 25, 2017