BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    OSTEONICS ION IMPLANT MOD-ML UNIKNEE FEMORAL COMP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNI LFIT MEDIAL FEMORAL COMP.

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code HRY·April 15, 2013

    INSTRUMENT DAMPING PORT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CT42 CARDIAC COMPUTED TOMOGRAPHY (CT) SOFTWARE

    FDA 510(k)
    FDA Class 2 ·Radiology

    LEVEL 1 HOTLINE LOW FLOW SYSTEMS

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LGZ·January 23, 2024

    LEVEL 1 HOTLINE LOW FLOW SYSTEMS

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LGZ·January 23, 2024

    5085 SURGICAL TABLE

    FDA Adverse Event
    STERIS CORPORATION - MONTGOMERY·Product code FQO·January 11, 2013

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·W.L. GORE & ASSOCIATES·Product code MIH·November 24, 2010

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 3, 2014