15 results · 22ms · Sources: EU EUDAMED, US FDA

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ARTHROSCOPE,RIGID ROD-LENS DIAGNOSTIC ENDOSCOPE

FDA 510(k)
FDA Class 2 ·Orthopedic

Wound Matrix TF

FDA 510(k)
FDA Unclassified ·Unknown

Nurochek-Pro System

FDA 510(k)
FDA Class 2 ·Neurology

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

PROPAQ MD DEFIBRILLATOR

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·January 8, 2013

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·January 2, 2011

MINICAP TRANSFER SET

FDA Adverse Event
Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·July 18, 2014

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