BEUDAMED
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    ACUMED CLAVICLE SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODEL 205GE-64: PATHWAY MRI CAROTID ARRAY COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    DUAL PORT WIZARD LOW PROFILE REPLACEMENT GASTROSTOMY DEVICE; DUAL PORT WIZARD FEEDING/DECOMPRESSION TUBE, MODEL 00220W

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ENDOTRACH TUBE 8229507 CONTACT EMG 7MM

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

    NIM® 3.0 INTERFACE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·November 29, 2017

    NIM® 3.0 MAINFRAME

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·June 16, 2017

    NIM® 3.0 MAINFRAME

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·December 8, 2017

    NIM® 3.0 MAINFRAME

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code GWF·August 30, 2016

    MAINFRAME 8253001 NIM RESPONSE 3.0

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·May 9, 2014

    ENDOTRACHEAL TUBE 8229307 NIM EMG 7MM RE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code ETN·May 10, 2013

    MAINFRAME 8253001 NIM RESPONSE 3.0

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code ETN·May 8, 2013

    NIM® 3.0 MAINFRAME

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·March 23, 2017

    NIM® 3.0 INTERFACE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·November 27, 2017

    ENDOTRACHEAL TUBE 8229306 NIM EMG 6MM RE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code ETN·May 10, 2013

    NIM® 3.0 MAINFRAME

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·April 21, 2016

    MAINFRAME 8253001 NIM RESPONSE 3.0

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·March 11, 2014

    NIM RESPONSE® 3.0 PATIENT INTERFACE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·July 22, 2014

    NIM RESPONSE® 3.0 PATIENT INTERFACE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·July 22, 2014

    MAINFRAME 8253001 NIM RESPONSE 3.0

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

    NIM-NEURO® 3.0 MAINFRAME

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·March 13, 2018