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

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    IMPLANTECH NASAL LABIAL IMPLANT

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

    RootMend MRR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    S.E.T. TUBE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PROFEMUR(R) MODULAR FEMORAL NECK

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code LWJ·July 27, 2015

    CVC KIT: 2-LUMEN 7FR X 2 0CM

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC·Product code DQY·December 3, 2010

    DURATA STS OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·July 18, 2014

    INFUSOMAT SPACE PUMP IV SET

    FDA Adverse Event
    Malfunction ·B. BRAUN DOMINICAN REPUBLIC·Product code FPA·November 17, 2009