BEUDAMED
    11 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    REBAR

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·September 7, 2021

    SOLITAIRE FR2

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·September 7, 2021

    REBAR

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·September 7, 2021

    SOLITAIRE FR2

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·September 7, 2021

    IMPLANT SYSTEM, FIBERTAK BUTTON

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MBI·May 9, 2024

    OPTIFLUX 160NRE DIALYZER FINISEHD ASSY

    FDA Adverse Event
    Malfunction ·OGDEN MANUFACTURING·Product code FJI·May 3, 2013

    STENOSCOP

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD. (GE PRIVATE)·Product code JAA·May 18, 2011

    COBAS INTEGRA 400

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·August 7, 2008

    SYRINGE 1ML LS SP120

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·September 16, 2021

    SYRINGE 1ML LS SP120

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·October 13, 2021

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·August 3, 2012