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

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    NASP TRANSPARENT DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    N/A

    FDA UDI
    MEDTRONIC NAVIGATION, INC.·00673978963211·CLAMPING RING 963-753 ZIEHM 12 II NL

    Needle Holder

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108390·ANIS NEEDLE HOLDER CURVED

    GFX NERVE ABLATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    FOUNDATIONS PLUS DOUBLE BAND EAR SUPPORT 3000

    FDA 510(k)
    FDA Class 1 ·General Hospital

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 7, 2014

    ASR UNI FEMORAL IMPL SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 15, 2013

    TEC 6 PLUS VAPORIZER

    FDA Adverse Event
    Malfunction ·GE DATEX OHMEDA·Product code CAD·January 11, 2011

    2.5 mm Reaming Rod W/Ball Tip 650 mm, Sterile

    FDA Enforcement
    Class II ·Terminated·Synthes (USA) Products LLC·November 30, 2016