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

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    MY BEAT POWERED TOOTHBRUSH

    FDA 510(k)
    FDA Class 1 ·Dental

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150775·K-WIRE - SINGLE TROCAR 2.0mm DIA x 230mm

    RAPID Graft Delivery

    FDA UDI
    Seaspine Orthopedics Corporation·10889981143046·Rectangular Funnel Pusher

    EMBOZENE COLOR-ADVANCED MICROSPHERES, EMBOZENE OPAQUE (NON-COLORED) MICROSPHERES, ONCOZENE MICROSPHERES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RESMED S8 PIONEER CPAP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    XMAX MOTOR

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code ERL·January 31, 2013

    ACUITY CENTRAL MONITORING

    FDA Adverse Event
    Malfunction ·WELCH ALLYN PROTOCOL, INC.·Product code DSI·December 9, 2010

    HA MLRY-HD POR LAT FMRL 11MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KXA·July 17, 2014