7 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Death
×
THERASPHERE
FDA Adverse Event
Death
·MDS NORDION·Product code KXK·May 12, 2003
THERASPHERE
FDA Adverse Event
Death
·MDS NORDION·Product code KXK·April 16, 2003
FUKUDA DENSHI MODEL LX3100
FDA Adverse Event
Death
·FUKUDA DENSHI CO., LTD.·Product code DSI·March 8, 2002
OXINET II CENTRAL STATION
FDA Adverse Event
Death
·NELLCOR PURITAN BENNETT·Product code DQA·April 2, 2002
ETHICON ENDOSURGERY INC.
FDA Adverse Event
Death
·ETHICON ENDOSURGERY INC·Product code GAG·March 26, 2002
NCP PULSE GENERATOR
FDA Adverse Event
Death
·CYBERONICS, INC.·Product code LYJ·July 3, 2002
VENTAK PRIZM HE DR 1853
FDA Adverse Event
Death
·GUIDANT CORP, CARDIAC RHYTHM MGMT·Product code LWS·July 26, 2002