8 results
·
17ms
·
Sources: EU EUDAMED, US FDA
DIESSE CRP TEST KIT
FDA 510(k)
FDA Class 2
·Immunology
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994806802·LID 1854221 SET SCREW MODULE LID
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209127351·
HMB ALLERGOGEN SKIN PRICK TEST NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
Optima Coil System (OptiOne Coil System)
FDA 510(k)
FDA Class 2
·Neurology
LIFEPAK(R) 12 DEFIBRILLATOR/MONITOR SERIES
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·June 6, 2014
VASOVIEW HEMOPRO 2
FDA Adverse Event
Injury
·MAQUET CARDIOVASCULAR, LLC·Product code GEI·November 29, 2012
TERUMO CDI 100 MONITOR
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTY·September 3, 2010