BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    ARROW BRACHIAL CENTRAL VENOUS CATH-KIT W/16GA & EC

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209126576·

    InQwire Amplatz Guide Wire

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CHIROPRACTIC ACTIVATOR OR PORT. CHIRO

    FDA 510(k)

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·June 6, 2014

    DIAL FLOWMETER

    FDA Adverse Event
    Malfunction ·PRECISION MEDICAL, INC·Product code CAN·November 9, 2012

    HUDSON NEBULIZER W/TEE

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CAF·September 3, 2010

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015