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

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    REFLECTIVE SPHERE STANDARD PROBE AND REFLECTIVE SPHERE DYNAMIC REFERENCE FRAME

    FDA 510(k)
    FDA Class 2 ·Neurology

    INnate Cannulated Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    I-PORTAL 4D VIDEO OCULOGRAPHY EYE TRACKING SYSTEM (VOG), I-PORTAL VIDEO NYSTAGMOGRAPHY SYSTEM (VNG), I-PORTAL NEURO OTOL

    FDA 510(k)
    FDA Class 2 ·Neurology

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP.·Product code NIQ·March 5, 2007

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP.·Product code NIQ·March 5, 2007

    ARTICULEZE M HEAD 36MM +8.5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code JDI·February 28, 2013

    UNKNOWN DEPUY MODULAR CATHCARTH HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·January 31, 2011

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    DANYANG MAXTHAI MEDICAL EQUIPMENT·Product code ITJ·August 6, 2014