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

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    MODIFICATION TO REFLEX AEC LINEAR STAPLER/CUTTER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    POWER DRIVE ART1 2304 WITH MOTOR HANDLES, TOOLS AND ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Hair Up

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    CELL-DYN 3700 SL ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·February 22, 2019

    FRESENIUS 2008K

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·June 25, 2014

    ESSURE

    FDA Adverse Event
    Injury ·CONCEPTUS, INC.·Product code HHS·February 20, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·February 7, 2011