BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    SYNTHES (USA) COMPACT AIR DRIVE II (CAD II)

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

    QC F/K-WIRES Ø0.6-3.2 F/532.001 532.010

    FDA Adverse Event
    Malfunction ·SYNTHES OBERDORF·Product code HWE·July 10, 2017

    TRYPTIC SOY AGAR WITH SHEEP BLOOD

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Arterys Viewer

    FDA 510(k)
    FDA Class 2 ·Radiology

    TRANSFER SET

    FDA Adverse Event
    Malfunction ·LIEBEL-FLARSHEIM CO.·Product code DXT·February 1, 2013

    LANX SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Injury ·LANX, INC.·Product code NKB·January 24, 2011

    M2A 38MM MOD HD+6MM NK NO SKRT

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 31, 2014