11 results
·
21ms
·
Sources: EU EUDAMED, US FDA
ND62T THYROID UPTAKE SYSTEM
FDA 510(k)
FDA Class 1
·Radiology
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704265866·
OPUS MAGNUM ANCHOR WITH INSERTER
FDA 510(k)
FDA Class 2
·Orthopedic
DICOMPACS DX-R WITH FLAT PANEL
FDA 510(k)
FDA Class 2
·Radiology
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·May 30, 2014
AUTOPULSE RESUSCITATION SYSTEM MODEL 100
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION, INC.·Product code DRM·October 23, 2012
HEART START XL
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code MKJ·September 16, 2010
MAGNUM HEAD
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·March 8, 2018
UNKNOWN STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·March 8, 2018
E-POLY LINER
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·March 8, 2018
CRUZ RT TRIFLANGE
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·March 8, 2018