BEUDAMED
    6 results · 75ms · Sources: EU EUDAMED, US FDA

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    NIM® EMG

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code ETN·February 5, 2016

    NICOLET EDX

    FDA Adverse Event
    Injury ·NATUS NEUROLOGY, INCORPORATED·Product code IKN·May 27, 2015

    Electromyography (EMG) needle electrodes

    Basic UDI-DI
    EU MDR · Eu Md Class 2a ·Spes Medica S.p.A.·126 devices

    DYON. CS RF-S WHIRLWIND 90 DEGREES PROBE

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORPORATION·Product code GEI·July 19, 2012

    DYONICS RF-S WHIRLWIND 90 DEGREES PROBE

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORPORATION·Product code GEI·July 19, 2012

    AXON PATIENT MODULE

    FDA Adverse Event
    Malfunction ·XOMED MFG JACKSONVILLE·Product code GWF·December 20, 2012