15 results · 21ms · 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.

PREPERITONEAL DISTENTION BALLOON SYSTEM

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

AUTO SUTURE MODIFIED ENDO STREAM SUC./IRRI. DEVICE

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

MEDICAL SUNLAMP FOR PHOTOTHERAPY

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

FLOGARD

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·January 30, 2013

HUDSON HCH, AQUA+

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code CAH·November 10, 2010

G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code MDS·July 15, 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