BEUDAMED
    7 results · 29ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION OF BIONECT HYDROGEL FOAM

    FDA 510(k)
    FDA Unclassified ·Unknown

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984267·anteriors; shade B1; mould 100

    OPUS MODELS 4033 AND 4034

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    ELECTRODE A.PH BLOOD GAS B.ELECTROLYTE SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    RIATA ST ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·February 28, 2013

    VOYAGER RX CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·February 10, 2011

    1.4MM X 12.8MM FLUTED ROUTER

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