7 results
·
16ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
GREENLIGHT XPS LASER SYSTEM
FDA Adverse Event
Injury
·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·March 4, 2014
PUMP MMT-522NAL PRDGM INS V2.2. CL EN
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code LZG·October 22, 2008
CONTAK RENEWAL
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 8, 2013
PALMAZ STENT UNKNOWN
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code FGE·May 13, 2013
EVOLUT PRO TRANSCATHETER AORTIC VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·April 22, 2024
PROGRAMMING HEAD
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code KRG·March 11, 2021
CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·April 25, 2022