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

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    SOUND VASER SYSTEM

    FDA 510(k)
    FDA Unclassified ·Unknown

    TranS1 Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PROVANT SYSTEM, MODEL 4201

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    ASR UNI FEMORAL IMPL SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·March 6, 2013

    CAPSURE Z NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014

    ARCHITECT C16000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·May 10, 2019