16 results
·
33ms
·
Sources: EU EUDAMED, US FDA
ARRHYTHMIA DETECTOR AND ALARM
FDA Adverse Event
Malfunction
·CARDIONET, INC·Product code DSI·April 21, 2009
ARRHYTHMIA DETECTOR AND ALARM
FDA Adverse Event
Malfunction
·CARDIONET, INC·Product code DSI·September 29, 2009
CARDIONET MONITOR
FDA Adverse Event
Malfunction
·CARDIONET, INC.·Product code DSI·February 22, 2009
EPATCH
FDA Adverse Event
Malfunction
·CARDIONET, INC·Product code DSI·September 19, 2018
CARDIONET
FDA Adverse Event
Injury
·CARDIONET, INC.·Product code DSI·February 6, 2018
BIOTEL HEART MONITOR DEVICE
FDA Adverse Event
Injury
·CARDIONET / LIFEWATCH / BIOTELEMETRY, INC.·Product code DSI·July 11, 2018
iMap Software
FDA UDI
Cardionxt Inc·00850012226338·
Multilink CS Catheter
FDA UDI
Cardionxt Inc·00850012226154·
iMap 3D Mapping and Navigation System
FDA UDI
Cardionxt Inc·00850012226291·
Axis Patient Patches
FDA UDI
Cardionxt Inc·00850012226000·
iMap Computer Cart
FDA UDI
Cardionxt Inc·00850012226406·
ER920W EVENT RECORDER
FDA Adverse Event
Malfunction
·BRAEMAR MANUFACTURING LLC·Product code DRG·October 26, 2016
ER920W EVENT RECORDER
FDA Adverse Event
Malfunction
·BRAEMAR MANUFACTURING, LLC·Product code DRG·April 24, 2015
ER920W EVENT RECORDER
FDA Adverse Event
Malfunction
·BRAEMAR MANFUACTURING, LLC·Product code DRG·December 1, 2015
ER920W EVENT RECORDER
FDA Adverse Event
Malfunction
·BRAEMAR MANUFACTURING, LLC·Product code DRG·December 20, 2016
3M RED DOT ELECTRODES
FDA Adverse Event
Other
·3M·Product code DRX·November 9, 2007