BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    SILON SILICONE TEXTILE COMPOSITE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704284638·SCALP CONTOUR RETRACTOR 5 1/2" 3X4 BLUNT

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·14026704920942·

    AEGIS ANTERIOR LUMBAR PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VantageTM Lumbar Decompression Kit

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC MILACA, INC.·Product code LWP·February 9, 2013

    DEXTRUS

    FDA Adverse Event
    Injury ·EXTERNAL MANUFACTURER·Product code NVN·January 7, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 23, 2014