7 results
·
27ms
·
Sources: EU EUDAMED, US FDA
OPUS RUBELLA TEST SYSTEM
FDA 510(k)
FDA Class 2
·Microbiology
MIO¿ ADVANCE
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·July 18, 2024
SCIMED OPTAMUM OPERATIVE PERIPHERAL ANGIOPLAS CATH
FDA 510(k)
FDA Class 2
·Cardiovascular
EDENTEC MODEL 3711 DIGITAL RECORDER
FDA 510(k)
FDA Class 2
·Cardiovascular
HS III PROXIMAL SEAL SYSTEM 4.3MM
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code DXC·June 12, 2014
CONSULTA
FDA Adverse Event
Death
·MEDTRONIC MED REL, INC.·Product code NIK·December 6, 2010
ACCESS® 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code MMI·January 15, 2013