BEUDAMED
    8 results · 23ms · Sources: EU EUDAMED, US FDA

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    ORTHO DX NEUROMUSCULAR STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    TheraBreath Dry Mouth Oral Rinse, TheraBreath Dry Mouth Lozenges

    FDA 510(k)
    FDA Unclassified ·Unknown

    DIGITAL STEREOLOC II

    FDA 510(k)
    FDA Class 2 ·Radiology

    QC F/K-WIRES Ø0.6-3.2 F/532.001 532.010

    FDA Adverse Event
    Malfunction ·SYNTHES OBERDORF·Product code HWE·July 10, 2017

    GREENLIGHT MOXY FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·August 5, 2015

    STARR SURGICAL - THE WAVE PHACO EMULSIFIED SYSTEM

    FDA Adverse Event
    Injury ·STARR SURGICAL·Product code HQC·June 25, 2007

    HARMONIC FOCUS* CURVED SHEAR 17CM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·July 31, 2014

    ENDOPATH ETS FLEX

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code KOG·March 24, 1997