25 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AECP-A, AUTOMATIC EXTERNAL COUNTERPULSATION DEVICE
FDA 510(k)
FDA Class 2
·Cardiovascular
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040009154·Zirlux 16+ A2 89x17x25
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033356487·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033356463·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033356456·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033356401·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033356470·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033356449·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033356494·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033356432·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033356395·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033356425·
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0112410·Awl Tap, 4.5 mm, Fixed Sleeve
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033356418·
ABBOTT VASCULAR PROGLIDE PERCLOSE
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR·Product code MGB·March 24, 2021
ACUMATCH P-SERIES PRESS-FIT PLASMA, ACUMATCH P-SERIES PRESS-FIT, ACUMATCH L-SERIES PRESS-FIT
FDA 510(k)
FDA Class 2
·Orthopedic
SHIMADZU WHOLE BODY X-RAY COMPUTED TOMOGRAPHY SCANNER SCT-7800TC
FDA 510(k)
FDA Class 2
·Radiology
ECAREMANAGER V3.6
FDA Adverse Event
Malfunction
·VISICU·Product code MSX·September 21, 2009
ECAREMANAGER V3.6
FDA Adverse Event
Malfunction
·VISICU·Product code MSX·December 14, 2009
PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code NIQ·August 7, 2009