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

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    ATTUNE® Porous Fixed Bearing Tibial Base, Medialized Dome Patella and Medialized Anatomic Patella with AFFIXIUM™ 3DP Technology

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    STRYKER CONSOLIDATED OPERATING ROOM EQUIPMENT (CORE) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    IMPLANET SPINE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·February 19, 2008

    VENACURE NEVERTOUCH

    FDA Adverse Event
    Malfunction ·ANGIODYNAMICS·Product code GEX·October 21, 2014

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·November 12, 2008

    ASR UNI FEMORAL IMPL SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·August 18, 2011