28 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ULTEGRA SYSTEM RAPID PLATELET FUNCTION ASSAY (RPFA)
FDA 510(k)
FDA Class 2
·Hematology
Zirlux
FDA UDI
HENRY SCHEIN, INC.·H65890113370·Zirlux Titanium Screw compatible with: Biomet 3...
Acculink™
FDA UDI
ABBOTT VASCULAR INC.·08717648076190·RX ACCULINK™ Carotid Stent System 5.0 mm x 30 m...
Acculink™
FDA UDI
ABBOTT VASCULAR INC.·08717648076183·RX ACCULINK™ Carotid Stent System 5.0 mm x 20 m...
Acculink™
FDA UDI
ABBOTT VASCULAR INC.·08717648076206·RX ACCULINK™ Carotid Stent System 5.0 mm x 40 m...
MedStream
FDA UDI
MEDICAL SPECIALTIES DISTRIBUTORS, LLC·00842472101157·DRESSING CHANGE KIT/CHG 1STEP/TEGFR/PF
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033274439·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033274408·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033296226·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033274415·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033357781·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033274446·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033274422·
Phonak
FDA UDI
Phonak AG·07613275066065·Phonak Bolero Q90-M312 (blue transparent)
LIPOPRINT SYSTEM, LDL SUBFRACTIONS
FDA 510(k)
FDA Class 1
·Clinical Chemistry
DANIELS SHARPSMART REUSABLE SHARPS CONTAINER
FDA 510(k)
FDA Class 2
·General Hospital
XACT CAROTID STENT SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR GALWAY·Product code NIM·April 22, 2008
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code MEB·September 17, 2021
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code MEB·September 4, 2024
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·May 14, 2018