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

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    EXTRAHAND BALLOON RETRACTOR

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690190615·Sizing Guide 3 deg Rotation Bushing -2mm

    PORTEX EPIDURAL CATHETER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Acuity 100 (hexafocon A) Rigid Gas Permeable Contact Lens

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    OPTUNE

    FDA Adverse Event
    Death ·NOVOCURE LTD·Product code NZK·May 29, 2015

    LIQUID FILLED RING TEETHER, MODEL 03807, LIQUID FILLED RING TEETHER, MODELS 1962005, 1962011, LIQUID FILLED TEETHING

    FDA 510(k)
    FDA Class 2 ·Dental

    PROMUS ELEMENT ¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·February 14, 2013

    EXCALIBUR, 5.5MM X 13CM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code GFA·January 17, 2011

    GORE VIATORR® TIPS ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIR·July 28, 2014