87 results · 30ms · Sources: EU EUDAMED, US FDA

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NIM 3.0

FDA 510(k)
FDA Class 2 ·Neurology

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

NIM PRASS PAIRED ELECTRODES

FDA Adverse Event
Injury ·MEDTRONIC XOMED INC.·Product code GXZ·November 20, 2014

NIM® 3.0 MAINFRAME INTERNATIONAL

FDA Adverse Event
Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·July 12, 2017