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

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    Filters Regulation: Us FDA ×

    OSTEOMED GREAT TOE SYSTEM

    FDA 510(k)
    FDA Unclassified ·Unknown

    APEX PS Knee

    FDA UDI
    Omni Life Science, Inc.·00841690113508·PS-C Insert, Size 2 x 11mm

    HLS UNI EVOLUTION PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYNTHES NAVIGABLE PEDICLE PREPARATION INSTRUMENTS

    FDA 510(k)
    FDA Class 2 ·Neurology

    NAVIGABLE HANDLE FOR USE WITH ACCESS CANNULA

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HAW·April 19, 2017

    STELLARIS 23G VITRECTOMY CUTTER

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB, INC.·Product code HQC·May 23, 2014

    DUROM ACETABULAR COMPONENT 50/44 J

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWY·January 15, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010