35 results
·
20ms
·
Sources: EU EUDAMED, US FDA
BRIDGE FX
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040012413·Zirlux 16+ A3.5 95X22
OneTouch Verio
FDA UDI
LifeScan Europe GmbH·00353885011556·OneTouch Verio Test Strips. For Blood glucose ...
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075737·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075720·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075669·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075683·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075751·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075713·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075652·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075744·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075706·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075690·
Battalion
FDA UDI
ALPHATEC SPINE, INC.·00840967186740·Battalion, LLIF Trial, 10°, 18 mm Wide, 17 mm X...
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075676·
PROMAX-XP, TENS AND MICROCURRENT DEVICE; PROMAX-TENS, TENS DEVICE; PROMAX-LIBRA, TENS DEVICE; PROMAX-MC, MICROCURRENT
FDA 510(k)
FDA Class 2
·Neurology
MX8000 V5.0 CT SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
SCREW LOCKING
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HWC·March 14, 2012
SCREW
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HWC·March 14, 2012
SCREW
FDA Adverse Event
Injury
·SYNTHES OBERDORF·Product code HWC·March 14, 2012