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

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    Filters FDA Adverse Event ×

    HEARTLIGHT

    FDA Adverse Event
    Injury ·CARDIOFOCUS·Product code OAE·November 26, 2018

    PIPELINE EMBOLIZATION DEVICE

    FDA Adverse Event
    Injury ·EV3 NEUROVASCULAR·Product code OUT·March 23, 2012

    PIPELINE EMBOLIZATION DEVICE

    FDA Adverse Event
    Injury ·EV3 NEUROVASCULAR·Product code OUT·June 30, 2014

    TENOR

    FDA Adverse Event
    Malfunction ·ARJOHUNTLEIGH POLSKA SP. ZO.O.·Product code FSA·May 31, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 5, 2011

    CARPENTIER- EDWARDS PERIMOUNT PLUS PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code LWR·August 27, 2008

    EVERFLEX+ SELF-EXPANDING PERIPHERAL STENT SYSTEM STANDARD

    FDA Adverse Event
    Injury ·COVIDIEN·Product code NIP·June 24, 2016

    PIPELINE EMBOLIZATION DEVICE

    FDA Adverse Event
    Injury ·EV3 NEUROVASCULAR·Product code OUT·January 17, 2014