BEUDAMED
    8 results · 17ms · Sources: EU EUDAMED, US FDA

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    LEMAITRE RETROGRADE VALVULOTOME

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981205621·Trial, 9mm x 24mm x 17mm, 10 Deg

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981191481·Interbody, 9mm x 24mm x 17mm, 10 Deg

    VIDAR BONE TRACK SYSTEM SOFTWARE

    FDA 510(k)
    FDA Class 2 ·Radiology

    SCIMED CARDIOTHERM CARDIOPLEGIA DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·December 14, 2010

    TENDRIL SDX

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·December 14, 2012