10,000 results
·
63ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
BIOSENSE WEBSTER
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER·Product code GXD·April 20, 2007
BIOSENSE WEBSTER
FDA Adverse Event
Malfunction
·Product code DQO·October 14, 2010
BIOSENSE WEBSTER
FDA Adverse Event
Malfunction
·STERILMED, INC.·Product code OWQ·August 18, 2020
BIOSENSE WEBSTER
FDA Adverse Event
Malfunction
·Product code OBJ·September 28, 2011
BIOSENSE WEBSTER
FDA Adverse Event
Malfunction
·Product code DRF·October 25, 2011
BIOSENSE WEBSTER
FDA Adverse Event
Malfunction
·ALLIANCE MEDICAL CORPORATION·Product code DRF·August 29, 2005
BIOSENSE WEBSTER CARTO
FDA Adverse Event
Malfunction
·JOHNSON & JOHNSON / BIOSENSE WEBSTER (ISRAEL), LTD.·Product code DQK·December 29, 2021
BIOSENSE WEBSTER CATHETER
FDA Adverse Event
Malfunction
·Product code DRF·October 25, 2011
BIOSENSE WEBSTER, INC.
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER, INC.·Product code DRF·June 10, 2011
BIOSENSE WEBSTER THERMOCOOL
FDA Adverse Event
Malfunction
·BIOSENSE·Product code LPB·June 20, 2017
BIOSENSE-WEBSTER E.P. CATHETER
FDA Adverse Event
Malfunction
·BIOSENSE-WEBSTER J&J CO.·Product code OAD·February 17, 2010
BIOSENSE WEBSTER SOUNDSTAR 3D
FDA Adverse Event
Malfunction
·ASCENT HEALTHCARE SOLUTIONS·Product code OBJ·May 9, 2010
BIOSENSE WEBSTER SOUNDSTAR 3D
FDA Adverse Event
Malfunction
·STRYKER SUSTAINABILITY SOLUTIONS·Product code OBJ·December 17, 2014
BIOSENSE WEBSTER LASSO CATHETER
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER, INC.·Product code DRF·April 24, 2007
BIOSENSE WEBSTER PREFACE SHEATH
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER, INC.·Product code DYB·December 22, 2006
BIOSENSE WEBSTER PREFACE SHEATH
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER, INC.·Product code DYB·December 22, 2006
BIOSENSE WEBSTER PREFACE SHEATH
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER, INC.·Product code DYB·December 22, 2006
BIOSENSE WEBSTER CARTO XP
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER·Product code DQK·June 30, 2006
BIOSENSE WEBSTER LASSO CATHETER
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code DRF·January 3, 2008
BIOSENSE WEBSTER PENTARAY NAV
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER, INC.·Product code MTD·January 16, 2020