46 results · 35ms · 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.

NEUROFEEDBACK

FDA Adverse Event
Injury ·EEG INFO·Product code HCC·February 24, 2016

NIHON KOHDEN NE-136A ELECTRODE

FDA Adverse Event
Injury ·NIHON KOHDEN CORPORATION·Product code GWQ·May 23, 2008

NUPREP GEL

FDA Adverse Event
Injury ·D.O. WEAVER AND CO·Product code GYB·March 29, 2007

ITREL II

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code LGW·November 2, 2009

AXON ECLIPSE INTRAOPERATIVE NEUROMONITOR 32 CHANNEL

FDA Adverse Event
Injury ·MEDTRONIC·Product code GWM·August 2, 2011

PROTECTIVE PLUS SAFETY IV CATHETER

FDA Adverse Event
Injury ·SMITHS MEDICAL·Product code FOZ·June 8, 2018

CYGNET EEG

FDA Adverse Event
Injury ·BEE SYSTEMS·Product code HCC·May 1, 2016

PULSE GEN MODEL 102

FDA Adverse Event
Injury ·CYBERONICS, INC.·Product code LYJ·April 22, 2010

ENTERRA

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code LNQ·June 19, 2009

PULSE GEN MODEL 102

FDA Adverse Event
Injury ·CYBERONICS, INC.·Product code LYJ·July 25, 2008

PULSE GEN MODEL 101

FDA Adverse Event
Injury ·CYBERONICS INC.·Product code LYJ·June 24, 2010

PULSE GEN MODEL 102

FDA Adverse Event
Injury ·CYBERONICS, INC.·Product code LYJ·October 14, 2009

RX ACCULINK CAROTID STENT SYSTEM

FDA Adverse Event
Injury ·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code NIM·December 3, 2008

SYNCHROMED II

FDA Adverse Event
Injury ·MEDTRONIC, INC., NEUROLOGICAL DIVISION·Product code LKK·January 18, 2007

PULSE GEN MODEL 102

FDA Adverse Event
Injury ·CYBERONICS, INC.·Product code LYJ·December 21, 2011

NUPREP GEL

FDA Adverse Event
Injury ·D. O. WEAVER AND COMPANY·Product code GYB·February 28, 2007

PULSE GEN MODEL 101

FDA Adverse Event
Injury ·CYBERONICS, INC.·Product code LYJ·April 1, 2011

PENTA

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·October 21, 2013

LIFECARE PCA 3

FDA Adverse Event
Injury ·HOSPIRA, INC.·Product code MEA·June 15, 2004

TEN20 CONDUCTIVE PASTE

FDA Adverse Event
Injury ·D. O. WEAVER AND COMPANY·Product code GYB·February 28, 2007