BEUDAMED
    6 results · 32ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 14, 2011

    11 GAUGE, T-GRIP ACCESS NEEDLES

    FDA Adverse Event
    Other ·ARTHROCARE CORP.·Product code GEA·January 29, 2008

    11 GAUGE CAVITY SPINEWAND

    FDA Adverse Event
    Other ·ARTHROCARE CORP.·Product code GEI·January 29, 2008

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS·Product code JAA·January 28, 2014

    ARTICULEZE M HEAD 36MM+8.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·October 3, 2012

    VERIFLEX (LIBERTE) CORONARY STENT DELIVERY SYSTEM

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC IRELAND LTD.·Product code MAF·July 25, 2010