BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    DYNAMIS™ SI Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO DYNESYS SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Surgical 3D Mask

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

    ENSEAL G2 ARTICULATING

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·November 11, 2014

    INFUSOMAT SPACE - US VERSION

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FRN·August 26, 2011

    SOLYX SIS SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·July 23, 2013

    BD Q-SYTE¿ LUER ACCESS SPLIT SEPTUM

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·August 15, 2019