BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    ALKALINE PHOSPHATASE

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209111305·KIT, CRISIS RESPONSE ORANGE- CUSTOM

    DEVICE CONNECTIVITY SOFTWARE DEVELOPERS KIT (SDK), MODEL 4500-900

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Pacel Bipolar Pacing Catheters

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 30, 2012

    HEARTSMART MRX

    FDA Adverse Event
    Malfunction ·Product code MKJ·September 25, 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