BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    TriVerity

    FDA 510(k)
    FDA Class 2 ·Microbiology

    RENOVIS SURGICAL POROUS ACETABULAR CUP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Barricaid Instrument Tray

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDI·November 10, 2014

    7600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·November 19, 2008

    INTRAVASCULAR SHUNT

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code DWF·July 22, 2013

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025