BEUDAMED
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    Lancing device

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

    Blade Handle

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112397·BARD-PARKER HANDLE #9

    THE TRABECULAR METAL MONOBLOCK CUP, MODELS 00-7259-0XX-28 (ZIMMER CAT. #) AND 02-293-28XX1 (IMPLEX PART #)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Schoelly Cystoscopes/Hysteroscopes and Accessories

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

    CAPTURE-R READY-SCREEN (4)

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·May 22, 2013

    M1 AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·August 17, 2011

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·November 3, 2014

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·July 5, 2013