31 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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COBE REVOLUTION
FDA 510(k)
FDA Class 2
·Cardiovascular
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040012543·Zirlux 16+ White 95X22
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0112350·Tap, 7.50mm, Fixed Sleeve
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077779·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077731·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077663·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077700·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077670·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077694·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077748·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077687·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077724·
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361011088·PedFuse RespondX, CNL, 6.0mm x 35mm
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077762·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077717·
POSI-GRIP UMBILICAL CORD CLAMP, STERILE, MODEL 384, POSI-GRIP UMBILICAL CORD CLAMP, NON-STERILE, MODEL 385
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
IRV2000 INDIVIDUAL RECREATIONAL VEHICLE
FDA 510(k)
FDA Class 2
·Physical Medicine
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