BEUDAMED
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    Q-SWEAT QUANTITATIVE SWEAT MEASUREMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    DISPSABLE FORCEPS, HEMOSTATS, PROBES, NEEDLE GUIDE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    POWDER FREE NITRILE (DARK BLUE) EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    LUMAX 340 DR-T

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code MRM·March 1, 2013

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 5, 2011

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·August 8, 2014

    Maquet Heartstring II Proximal Seal System (HS-1045) manufactured by Maquet Cardiovascular, Wayne, NJ Intended use: medical device for use by cardiac surgeons during CABG procedures to maintain hemostasis and to facilitate the completion of a proximal anastomosis without application of an aortic clamp.

    FDA Recall
    Terminated ·Maquet Cardiovascular, LLC·Product code DXC·May 5, 2010