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

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    PULSE*SPRAY INFUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00681490847056·INSTRUMENT 8951602 16 12MM STD STYL DIST

    Alphenix, INFX-8000V/B, INFX-8000V/S, V9.6 with aEvolve Imaging

    FDA 510(k)
    FDA Class 2 ·Radiology

    AXIOM SIRESKOP SD

    FDA 510(k)
    FDA Class 2 ·Radiology

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO·Product code LWS·February 9, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2014

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 6, 2011