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

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    ZIDA Wearable Neuromodulation System

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    VIBRO-TRAC

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    DIGIFIX EXTERNAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INTEGRA DP PEDIATRIC BURR HOLE SYSTEM

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCICENCS IMPLANTS SA·Product code JXG·June 15, 2016

    E.COM, SYMBIA E

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SOLUTIONS USA, INC. MI GROUP·Product code IYX·March 15, 2012

    E.CAM

    FDA Adverse Event
    Injury ·SIEMENS MEDICAL SOLUTIONS USA, INC. MI GROUP·Product code KPS·January 7, 2014

    SYMBIA T-SERIES

    FDA Adverse Event
    Injury ·SIEMENS MEDICAL SOLUTIONS USA, INC. MI GROUP·Product code KPS·September 20, 2013

    E. CAM COMPUTER [510(K) K992731]

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS, INC.·Product code IYX·April 20, 2001

    PROMUS ELEMENT? PLUS

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·June 27, 2013

    AIR DERMATOME KIT

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code GFD·July 20, 2011

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·October 22, 2014