BEUDAMED
    8 results · 28ms · Sources: EU EUDAMED, US FDA

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    EVITA 2 DURA

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970165·anteriors; shade B1; mould UCM

    ENSEAL PTC TRIO

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Osteo-P Bone Graft Substitute

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LUMBER INTERBODY FUSION SYSTEM INSTRUMENTATION

    FDA Adverse Event
    Injury ·CENTERPULSE SPINE-TECH·Product code LXH·December 11, 2003

    BATTERY 14.8V, 6.3 AH LI-ION BATTERY

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 29, 2014

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·February 20, 2013

    VERSAFITCUP DOUBLE MOBILITY LINER

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·January 14, 2011