8 results
·
26ms
·
Sources: EU EUDAMED, US FDA
ULTRATHERM (908)
FDA 510(k)
FDA Class 2
·Physical Medicine
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471122956·K-WIRE - SINGLE TROCAR 0.8mm DIA x 75mm
RUBEOLA IGM ELISA TEST
FDA 510(k)
FDA Class 1
·Microbiology
GAMBRO BICARBONATE MONITOR BCM 10-2
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
BD CONNECTA¿ STOPCOCKS
FDA Adverse Event
Injury
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMG·June 30, 2016
HEARTSTART XL+ DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 22, 2014
CARPENTIER-EDWARDS PERIMOUNT PLUS PERICARDIAL BIOPROSTHESIS
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·February 15, 2013
SHUNT SENSOR SYS500
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·December 20, 2010