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

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    SYNERGY(TM) TI POSTERIOR SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BASE

    FDA UDI
    Nuvasive, Inc.·00887517707512·BASE Centering Pin

    HAMMERTOE PIN DRIVER

    FDA UDI
    Biomet Orthopedics, LLC·00880304416635·

    SIGMA 5000 SERIES IMAGIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    Depuy Synthes Variable Angle Locking Hand System (1.3 mm and 2.0 mm Plates and Screws)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES GRENCHEN·Product code HRS·January 30, 2017

    DASHER -14 STEERABLE GUIDEWIRE

    FDA Adverse Event
    Injury ·NEUROVASCULAR, A DIVISION OF BOSTON SCIENTIFIC CORP·Product code DQX·January 9, 2007

    HYPERFORM OCCLUSION BALLOON SYSTEM

    FDA Adverse Event
    Malfunction ·EV3 NEUROVASCULAR·Product code MJN·February 8, 2013

    ACCURUS 800CS

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·December 7, 2010

    COR/TRI ANT STEM INSERT SHAFT

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LXH·July 22, 2014