BEUDAMED
    8 results · 23ms · Sources: EU EUDAMED, US FDA

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    PEEK CAGE FOR THE VERTEBRAL SPINE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DURAGEN XS DURAL REGENERATION MATRIX 2X2 GRAFT

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES CORPORATION·Product code GXQ·October 24, 2016

    DURAGEN SUTURABLE DURAL REGENERATION TEMPLATE 2

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES CORPORATION·Product code GXQ·October 24, 2016

    MODIFICATION TO: AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BABI PLUS NEONATAL RESUSCITATION BAG

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·October 1, 2014

    SMALL PERIPHERAL CUTTING BALLOON?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code LOX·May 29, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 17, 2011