BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Pinpoint GT Introducer Needle

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PRESSUREWIRE CERTUS, MODELS 12006 AND 12306

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NEODENT IMPLANT FOR ORTHODONTIC ANCHORAGE

    FDA 510(k)
    FDA Class 2 ·Dental

    NUCLEUS FREEDOM IMPLANT WITH CONTOUR ADVANCE ELECTRODE

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·March 4, 2020

    QUICK-RELEASE SELF-HOLDING SCREWDRIVER

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code LXH·June 11, 2013

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·July 14, 2011

    HALL SURGICAL BUR GUARD, MEDIUM

    FDA Adverse Event
    Malfunction ·LINVATEC CORP.·Product code HTT·September 8, 2008