BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    VPW2877E7 X RAY POWER SUPPLY

    FDA 510(k)
    FDA Class 1 ·Radiology

    ACL CROSSPIN

    FDA UDI
    Biomet Sports Medicine, LLC·00880304421301·

    Lucitone® FRS®

    FDA UDI
    Dentsply International Inc.·D0019058550·

    NEW JERSEY TOTAL SHOULDER GLENOID COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LATEX PATIENT EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MP70 INTELLIVUE PATIENT MONITOR

    FDA Adverse Event
    Death ·PHILIPS MEDICAL SYSTEMS·Product code DSI·November 18, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 9, 2013

    2520274-2013-10113

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWQ·November 2, 2013