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

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    Filters FDA Adverse Event ×

    OLYMPUS

    FDA Adverse Event
    Malfunction ·OLYMPUS·Product code FDF·June 10, 2013

    COGNIS

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 20, 2011

    PINNACLE MTL INS NEUT40IDX58OD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·October 14, 2014

    IMPELLA RP PUMP

    FDA Adverse Event
    Malfunction ·ABIOMED, INC.·Product code OZD·February 6, 2020

    PIPELINE FLEX W/SHIELD TECHNOLOGY

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·May 14, 2021

    PIPELINE FLEX W/SHIELD TECHNOLOGY

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·June 3, 2021

    PIPELINE FLEX W/SHIELD TECHNOLOGY

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·May 6, 2021

    PIPELINE FLEX W/SHIELD TECHNOLOGY

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·June 8, 2021

    PIPELINE FLEX W/SHIELD TECHNOLOGY

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·June 11, 2021

    ACCUDRAIN WITH ANTI-REFLUX VALVE

    FDA Adverse Event
    Injury ·INTEGRA NEUROSCIENCES PR·Product code JXG·January 4, 2018

    ACCUDRAIN WITH ANTI-REFLUX VALVE

    FDA Adverse Event
    Injury ·INTEGRA NEUROSCIENCES PR·Product code JXG·January 23, 2018