7 results
·
17ms
·
Sources: EU EUDAMED, US FDA
RMI SOFCLAMP
FDA 510(k)
FDA Class 2
·Cardiovascular
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471122826·K-WIRE - DOUBLE TROCAR 0.7mm DIA x 150mm
Blood Pressure Monitor
FDA 510(k)
FDA Class 2
·Cardiovascular
S-250 PROTON BEAM RADIATION THERAPY SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
MENISCAL CINCH, CURVED TIP
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code GAT·December 13, 2010
ENDURON 10D 52OD X 28ID
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·January 17, 2013
ALLURE QUADRA RF
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·July 8, 2014