BEUDAMED
    6 results · 23ms · Sources: EU EUDAMED, US FDA

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    FOUNDATION NON-POROUS STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REPLACEMENT RECHARGEABLE BATTERY PACK'S

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ELECTROSONOGRAM ESG-1

    FDA 510(k)
    FDA Class 1 ·Dental

    GOBED II

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·January 4, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HLTHCARE CORP·Product code FRN·February 3, 2014

    ENDEAVOR SPRINT RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·November 10, 2010