BEUDAMED
    16 results · 26ms · Sources: EU EUDAMED, US FDA

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    NERVE INTEGRITY MONITOR-2 (NIM-2 XL)

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    MAINFRAME 8253001 NIM RESPONSE 3.0

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC·Product code ETN·November 7, 2013

    NIM® EMG - ENDOTRACHEAL TUBE - TRIVANTAGE®

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·June 3, 2015

    MAINFRAME 8253001 NIM RESPONSE 3.0

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC·Product code ETN·December 16, 2013

    NIM® 3.0 MAINFRAME

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code ETN·January 14, 2015

    ENDOTRACH TUBE 8229507 CONTACT EMG 7MM

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code ETN·January 7, 2014

    NIM® EMG ELECTRODE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code GXZ·January 27, 2017

    NIM® EMG - ENDOTRACHEAL TUBE - TRIVANTAGE®

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC·Product code ETN·July 1, 2016

    NIM® EMG - ENDOTRACHEAL TUBE - TRIVANTAGE®

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·December 8, 2016

    NIM® EMG ELECTRODE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code GXZ·February 13, 2017

    PullUp Probe Cover Kit

    FDA UDI
    PROTEK MEDICAL PRODUCTS, INC.·00841912100156·

    PANOSOL II UVA-218

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    LOEFFLER MEDIUM TUBE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    TERUMO STERNAL SAW II

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEM CORP·Product code GFA·January 11, 2013

    VANGUARD LOCK-ON FEMORAL IMPACTOR

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code HWA·November 23, 2010

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·July 15, 2014