BEUDAMED
    7 results · 33ms · Sources: EU EUDAMED, US FDA

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    SPACELABS MODEL 90480 EEG MODULE

    FDA 510(k)
    FDA Class 2 ·Neurology

    BREATH TRACKER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PATIENT EXAM GLOVES (MFG. JENQ CHUAM INDUSTRIAL)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·June 26, 2014

    MEDTRONIC INFUSE BONE GRAFT OR RHBMP2

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NEK·January 3, 2013

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·November 11, 2010

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021