15 results · 21ms · Sources: EU EUDAMED, US FDA

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SBP DENTAL UNIT

FDA 510(k)
FDA Class 1 ·Dental

CHEMONUCLEOLYSIS NEEDLE

FDA 510(k)
FDA Class 2 ·General Hospital

QUICKANCHOR (TM)

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

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

NATURALYTE

FDA Adverse Event
Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 27, 2014

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 24, 2010

TERUMO ADVANCED PERFUSION SYSTEM 1

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·January 11, 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