BEUDAMED
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    Revital-Ox RESERT Solution Test Strip

    FDA 510(k)
    FDA Class 2 ·General Hospital

    E.M Adams co, inc.

    FDA UDI
    E.M. ADAMS, INC.·10840200301517·SINGLE INSTRUMENT

    E.M Adams co, inc.

    FDA UDI
    E.M. ADAMS, INC.·18100013401517·SINGLE INSTRUMENT

    VITREA2, VERSION 3.7 MEDICAL IMAGE PROCESSING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    KIMBERLY-CLARK KIM VENT MICROCUFF ENDOTRACHEAL TUBE FOR ADULTS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 6, 2025

    OBTAPE TRANSOBTURATOR SLING

    FDA Adverse Event
    Injury ·MENTOR WORLDWIDE LLC·Product code FTL·May 23, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·September 27, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 29, 2011

    TENSION FREE VAGINAL TAPE - ABBREVO UNKNOWN PROD

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·October 29, 2019