BEUDAMED
    8 results · 27ms · Sources: EU EUDAMED, US FDA

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    MOBILE X-RAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909135252·REVELATION DIAMOND 877K-016M - 5 PACK

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962159293·BLUNT OBTURATOR FOR 2.5MM OPERATING SHEATH, COL...

    ACTIVECARE DVT ACTIVECARE+SFT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CONTREET-H ANTIMICROBIAL HYDROCOLLOID DRESSING, MODELS 9610 (4 X 4 (10 CM X 10CM), 9613 (6X6 (15CM X 15CM)

    FDA 510(k)
    FDA Unclassified ·Unknown

    PROSTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code KNS·November 12, 2010

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 3, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 21, 2012