BEUDAMED
    6 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Scorpio Universal Dome Patella; Scorpio Total Stabilizer Insert; Scorpio-Flex Posterior Stabilized Tibial Insert; Scorpio-Flex Cruciate Retaining Tibial Insert; Scorpio NRG Tibial Bearing Insert – Cruciate Retaining Insert; Scorpio NRG Tibial Bearing Insert – Posteriorly Stabilized Insert

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MPO Knee Instruments; MPO PROPHECY Knee Instruments

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Tyber Medical Anatomical Plating System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ONETOUCH ULTRASMART METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·November 24, 2008

    EXETER V40 STEM 50MM NO 1

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code JDI·September 6, 2011

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·July 23, 2013