14 results · 63ms · Sources: EU EUDAMED, US FDA

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NAVISTAR® THERMOCOOL®

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code OAD·August 26, 2014

INQUIRY OPTIMA DIAGNOSTIC CATHETER

FDA Adverse Event
Injury ·IRVINE BIOMEDICAL, INC.(IBI)·Product code DRF·January 11, 2007

INQUIRY OPTIMA STEERABLE DIAGNOSTIC CATHETER

FDA Adverse Event
Malfunction ·IRVINE BIOMEDICAL, INC. (IBI)·Product code DRF·January 27, 2006

INQUIRY OPTIMA STEERABLE DIAGNOSTIC CATHETER

FDA Adverse Event
Malfunction ·IRVINE BIOMEDICAL, INC. (IBI)·Product code DRF·January 23, 2006

INQUIRY OPTIMA STEERABLE DIAGNOSTIC CATHETER

FDA Adverse Event
Malfunction ·IRVINE BIOMEDICAL, INC. (IBI)·Product code DRF·February 13, 2006

INQUIRY OPTIMA STEERABLE DIAGNOSTIC CATHETER

FDA Adverse Event
Malfunction ·IRVINE BIOMEDICAL INC. (IBI)·Product code DRF·February 13, 2006

INQUIRY OPTIMA STEERABLE DIAGNOSTIC CATHETER

FDA Adverse Event
Malfunction ·IRVINE BIOMEDICAL, INC. (IBI)·Product code DRF·November 23, 2005

INQUIRY OPTIMA STEERABLE DIAGNOSTIC CATHETER

FDA Adverse Event
Malfunction ·IRVINE BIOMEDICAL, INC. (IBI)·Product code DRF·November 4, 2005

INQUIRY OPTIMA STEERABLE DIAGNOSTIC CATHETER

FDA Adverse Event
Malfunction ·IRVINE BIOMEDICAL INC. (IBI)·Product code DRF·November 4, 2005

INQUIRY AFOCUS II DIAGNOSTIC CATHETER

FDA Adverse Event
Malfunction ·IRVINE BIOMEDICAL, INC.(IBI)·Product code DQO·April 14, 2006

INQUIRY 1100 SERIES DIAGNOSTIC CATHETER

FDA Adverse Event
Injury ·IRVINE BIOMEDICAL, INC. (IBI)·Product code DRF·June 11, 2004

THERAPY DUAL 8 ABLATION CATHETER

FDA Adverse Event
Malfunction ·IRVINE BIOMEDICAL, INC. (IBI)·Product code DRF·August 16, 2005

CARDIAC ABLATION GENERATOR

FDA Adverse Event
Malfunction ·IRVINE BIOMEDICAL, INC. (IBI)·Product code DRF·August 17, 2006

INQUIRY DIAGNOSTIC CATHETER

FDA Adverse Event
Malfunction ·IRVINE BIOMEDICAL, INC (IBI), A ST JUDE MEDICAL COMPANY·Product code DQO·October 14, 2008