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

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    AMBULATORY X-12 TELEMETRY MODULE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FLEXISYS

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

    FALSE RAGWEED ALLERGEN DISC

    FDA 510(k)
    FDA Class 2 ·Immunology

    BD VACUTAINER® K2 EDTA (K2E) 10.8 MG BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·May 22, 2018

    PENUMBRA SYSTEM REPERFUSION CATHETER 032

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·February 22, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 1, 2014