BEUDAMED
    8 results · 24ms · Sources: EU EUDAMED, US FDA

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    LIFEPORT VASCU ACCESS SYST/PORT INTRO KIT 7015

    FDA 510(k)
    FDA Class 2 ·General Hospital

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909113552·REVELATION DIAMOND 859-016UF - 5 PACK

    Maestro®

    FDA UDI
    Ortho Organizers, Inc.·00190707047214·.022 LR6 NC Std -30T 2A 0O

    ECHOBRIGHT

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BIOLIGHT PCD

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    X8000 LIGHTSOURCE

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY SAN JOSE·Product code FCW·November 23, 2010

    TRANSVENOUS

    FDA Adverse Event
    Injury ·HISTORICAL PUERTO RICO·Product code NVN·January 11, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 3, 2014