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

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    SKINCOTE

    FDA 510(k)
    FDA Unclassified ·Unknown

    STRYKER COMPARTMENTAL KNEE SYSTEM LINE EXTENSION

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RELIEF

    FDA 510(k)
    FDA Unclassified ·Unknown

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·June 19, 2014

    LTV

    FDA Adverse Event
    Injury ·CAREFUSION 203, INC·Product code CBK·October 22, 2010

    PROMUS ELEMENT¿ PLUS

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·December 20, 2012

    BIOLOX® DELTA, CERAMIC FEMORAL HEAD, S, 36/-3.5, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·February 21, 2017