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

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    ULTRACK TOTAL KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PathLoc-C Posterior Cervical Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODEL 43130A DEFIBRILLATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SPRINT QUATTRO

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·February 9, 2013

    NXSTAGE SYSTEM ONE

    FDA Adverse Event
    Injury ·NXSTAGE MEDICAL, INC.·Product code KDI·December 30, 2010

    DHS®/DCS® COUPLING SCREW

    FDA Adverse Event
    Malfunction ·SYNTHES HAGENDORF·Product code HWB·July 23, 2014