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