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

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    CONSENSUS KNEE SYSTEM - PRIMARY KNEE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HL888BM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LINA POWERBLADE PLUS

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

    ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Death ·WARSAW ORTHOPEDIC, INC.·Product code KWQ·January 29, 2013

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·December 20, 2010

    CVC KIT: 2-LUMEN 7FR X 20 CM

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DQY·March 11, 2014