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

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    ULTRAPAK E

    FDA 510(k)
    FDA Unclassified ·Unknown

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981596·anteriors; shade A3.5 light; mould CM4

    Spine Wave Navigated Instruments

    FDA 510(k)
    FDA Class 2 ·Neurology

    HEARING AID, MODEL 775 PP/AGC

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·February 27, 2013

    TERUMO CDI 500 BLOOD PARAMETER MONITOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·January 31, 2011

    STERILIZATION CASE & TRAY, XMAX

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·December 18, 2013