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

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

ZEISS 20 SL SLIT-LAMP & MECHANICAL MICROMANIPULATR

FDA 510(k)
FDA Class 2 ·Ophthalmic

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613035471·Nichamin Quick Chopper, Angled 10mm Bend To Tip...

ZIRCONIA CERAMIC MODULAR HEAD 9TYPE II TAPER

FDA 510(k)
FDA Class 2 ·Orthopedic

FST CATH-UD CATHETER

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

ENDOTRACHEAL TUBE 7.5 MM EMG FLEX

FDA Adverse Event
Injury ·MEDTRONIC XOMED, INC.·Product code BTR·July 28, 2010

MAINFRAME 8253001 NIM RESPONSE 3.0

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

3002 MASTER BOMS

FDA Adverse Event
Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·January 22, 2013

ASKU

FDA Adverse Event
Injury ·MEDTRONIC MILACA INC.·Product code DTE·December 14, 2010

QUARTET

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code OJX·July 10, 2014

ENDOTRACH TUBE 8229306J NIM EMG 6MM

FDA Adverse Event
Malfunction ·MEDTRONIC XOMED, INC·Product code ETN·March 6, 2013

ENDOTRACHEAL TUBE 8229307 NIM EMG 7MM RE

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

ENDOTRACH TUBE 8229980 5PK 8MM EMG FLEX

FDA Adverse Event
Injury ·MEDTRONIC XOMED, INC.·Product code ETN·March 11, 2013

MAINFRAME 8253001 NIM RESPONSE 3.0

FDA Adverse Event
Malfunction ·MEDTRONIC XOMED, INC.·Product code ETN·August 26, 2013

ENDOTRACH TUBE 8229980 5PK 8MM EMG FLEX

FDA Adverse Event
Malfunction ·MEDTRONIC XOMED, INC.·Product code ETN·February 11, 2013

NIM® EMG - ENDOTRACHEAL TUBE - NIM FLEX¿

FDA Adverse Event
Injury ·MEDTRONIC XOMED INC.·Product code ETN·October 18, 2021

MAINFRAME 8253001 NIM RESPONSE 3.0

FDA Adverse Event
Malfunction ·MEDTRONIC XOMED, INC.·Product code ETN·August 28, 2013