BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    OPHTA SIL (RITLENG PROBE AND LACRIMAL INTUBATION SET)

    FDA 510(k)
    FDA Unclassified ·Unknown

    XLIF

    FDA UDI
    Nuvasive, Inc.·00887517840783·XLIF XL Paddle Sizer, 8mm Bullleted

    FIXOS

    FDA UDI
    Stryker GmbH·07613327083217·Drawer Tag - 5.0 mm Instruments

    VITALAB MAGNESIUM REAGENT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    ZIMMER PLATES AND SCREWS SYSTEM(ZPS)- NON-STERILE PLATES AND SCREWS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    6F ANGIO-SEAL VASCULAR CLOSURE DEVICE STS PLUS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code MGB·December 21, 2010

    GREENLIGHT MOXY FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·July 17, 2014

    MAXGUARD SECONDARY SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP·Product code FPA·December 19, 2012