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

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    FOUNDATION GLENOID COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295234500·P.F.C. SIGMA POSTERIOR AUGMENT COMBO CEMENTED S...

    ENDOPATH ENDOSCOPIC MULTIFEED STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·December 10, 1996

    CALYPSO 4D LOCALIZATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    Rampart O Lumbar Interbody Fusion Device, Rampart T Lumbar Interbody Fusion Device, Rampart A lumbar Interbody Fusion Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·February 11, 2013

    SILVERHAWK® PLAQUE EXCISION SYSTEM

    FDA Adverse Event
    Injury ·EV3 INC. PLYMOUTH, MN·Product code MCW·January 14, 2011

    PENTA

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL -NEUROMODULATION·Product code GZB·July 22, 2014

    ENDOPATH ENDOSCOPIC VASCULAR LINEAR CUTTER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·September 10, 1996