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

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    REUSABLE FINGER CLIP RECORDING ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Neurology

    SwishPlus® Implant

    FDA UDI
    IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307106289·5.7mmD x 6mmL, 6.5mmD Platform

    Control The Bleed Premium - Back Pack 5243

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588257068·Control The Bleed Premium - Back Pack 5243

    GYN-1500 HYSTEROSCOPIC INUFFLATOR

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    LIPASE REAGENT SET

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    OT VERIO IQ METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 22, 2013

    ATTAIN ABILITY

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code OJX·December 14, 2010

    ZEPHYR XL SR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·July 10, 2014