BEUDAMED
    7 results · 28ms · Sources: EU EUDAMED, US FDA

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    OMNIFIT(R) TOTAL KNEE SYSTEM (MODIFICATION)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NA

    FDA UDI
    KEY SURGICAL, INC.·10849771050213·Steinmann Pins, Double trocar threaded, 0.189-i...

    Straumann PURE Ceramic Implants

    FDA 510(k)
    FDA Class 2 ·Dental

    TINNITUS MASKERS, MODELS S564&S574

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 13, 2014

    COLLEAGUE CXE VOLUMETRICINFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 15, 2010

    ASR UNI FEMORAL IMPL SIZE 55

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·December 13, 2012