BEUDAMED
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    VERIFY® Chemical Indicator for SYSTEM 1E® and SYSTEM 1® endo Liquid Chemical Sterilant Processing Systems

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SCENIUM

    FDA 510(k)
    FDA Class 2 ·Radiology

    FORCE FIBER

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

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code NIQ·September 18, 2006

    SENSOR ENLITE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OZO·November 6, 2014

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 2, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 18, 2013