BEUDAMED
    7 results · 33ms · Sources: EU EUDAMED, US FDA

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    MANUAL RONGEUR

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    4874954

    FDA Adverse Event
    Malfunction ·June 26, 2015

    MODEL NUMBER 9216 RESPIRATION/HEART RATE MONITOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ABUTMENT HEAD POST

    FDA 510(k)
    FDA Class 2 ·Dental

    HEARTSTART FRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 25, 2014

    SM304 M-SERIES W/ZOOM

    FDA Adverse Event
    Malfunction ·STRYKER CORP. MEDICAL DIVISION·Product code INK·October 13, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 16, 2012