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

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    K-CAP-I ORTHOPEDIC FIXATION WIRE CAP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Elite®

    FDA UDI
    Ortho Organizers, Inc.·00190707051464·.018 L6R DBT/NC 0T 5 OFF

    MAXIMA-M STRAIGHT ATTACHMENT, MAXIMA-M CONTRA ANGLE SHEATH

    FDA 510(k)
    FDA Class 1 ·Dental

    NAVITRAK SYSTEM-OPTICAL OPTION, MODEL 900.004

    FDA 510(k)
    FDA Class 2 ·Neurology

    ASR ACETABULAR CUPS 54

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·November 10, 2010

    PENA MUSCLE STIMULATOR PROBE (NOT STERILE)

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCIENCES IMPLANTS S.A.·Product code IPF·February 24, 2014

    LIGASURE IMPACT THORACIC

    FDA Adverse Event
    Malfunction ·COVIDIEN LLC (SHANGHAI)·Product code GEI·November 27, 2012