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

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    Genesys Spine Apache® Anterior Lumbar Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138111·Trial, 38 X 30, 21mm Height 22° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138081·Trial, 38 X 30, 15mm Height 22° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138098·Trial, 38 X 30, 17mm Height 22° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138104·Trial, 38 X 30, 19mm Height 22° Hyperlordotic

    ULTRAEZ DESENSITIZING GEL

    FDA 510(k)
    FDA Class 2 ·Dental

    T2 GREATER TROCHANTER NAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 5, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 14, 2011

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·October 10, 2014

    NIM®

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code ETN·June 27, 2016

    ANALYTICAL E MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·September 28, 2011