BEUDAMED
    8 results · 24ms · Sources: EU EUDAMED, US FDA

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    MARCO TRIAL SETS

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    EDENTA

    FDA UDI
    EDENTA ETABLISSEMENT·E312K90044610001·Dowel Pin 12 mm

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515309869·Joseph Periosteal Elevator, slightly curved, 2m...

    REPICCI LOCKED KEEL TIBIAL BEARING

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FASTBRACES CERAMIC BRACKETS

    FDA 510(k)
    FDA Class 2 ·Dental

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·December 16, 2010

    UNKNOWN ZIMMER HIP

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code KWY·January 23, 2013

    AUTOPULSE® RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC·Product code DRM·July 11, 2014