BEUDAMED
    4 results · 35ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    K-WIRE, RECON 3.2X400 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·June 29, 2011

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LGW·January 25, 2013

    FEMORAL PLATE 15 HOLE RIGHT

    FDA Adverse Event
    Malfunction ·DEPUY ACE S.A. 'R.L.·Product code HRS·November 24, 2010

    XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·July 11, 2014