5 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
M2A-MAGNUM MOD HD SZ 52MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·November 8, 2017
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·June 25, 2014
MINICAP TRANSFER SET
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·January 3, 2013
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code NIQ·November 5, 2010
PAEDIATRIC CANNULA, VENOUS
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA·Product code DWF·June 7, 2023