BEUDAMED
    8 results · 29ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    S-ROM*SLEEVE PRX ZTT, 18B-SML

    FDA Adverse Event
    Injury ·9616671 DEPUY IRELAND·Product code LPH·October 10, 2013

    S-ROM M 28MM HEAD +6

    FDA Adverse Event
    Injury ·8010379 DEPUY INTL., LTD.·Product code JDI·October 10, 2013

    PINNACLE SECTOR II CUP 48MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC·Product code KWA·October 10, 2013

    SROM*STM ST,30+4L NK,18X13X160

    FDA Adverse Event
    Injury ·9616671 DEPUY IRELAND·Product code JDI·October 10, 2013

    ULTAMET MTL INS NEUT 28MM 48OD

    FDA Adverse Event
    Injury ·8010379 DEPUY INTL., LTD.·Product code KWA·October 10, 2013

    VITALITY DS

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·November 11, 2008

    HOMECHOICE

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·September 19, 2011

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·July 30, 2013