308 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MODIFICATION TO STANDARD HUMAN PLASMA
FDA 510(k)
FDA Class 2
·Hematology
Stryker
FDA UDI
Provision·00810041637185·
ConMed
FDA UDI
Provision·B504OM50231410·
Stryker
FDA UDI
Provision·B504OM60231410·
PROFYLE
FDA UDI
Stryker GmbH·07613154345564·DRILL, WL 40MM, STRYKER-SHAFT
MedSource Silk/Cloth Tape
FDA UDI
MEDSOURCE INTERNATIONAL LLC·00816703023457·Silk/Cloth Tape 1x2.5 yards
NA
FDA UDI
Conmed Corporation·10845854003688·MICRO SAGITTAL BLADE, FINE, 6 X 34 X 0.4 MM
NA
FDA UDI
STERILMED, INC.·10888551019453·SAW BLADE SAGITTAL FINE TOOTH
MICROGYN PLUS STIMULATION DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
UBM PLUS, MODEL P45
FDA 510(k)
FDA Class 2
·Radiology
ABUTMENT: SHOULDERED, 5MM, INTEGRAL, 3.25
FDA Adverse Event
Injury
·SULZER CALCITEK·Product code DZE·August 4, 1998
ABUTMENT: SHOULDERED, 3MM, INTEGRAL, 3.25
FDA Adverse Event
Injury
·SULZER CALCITEK·Product code DZE·August 4, 1998
ABUTMENT: SHOULDERED, 4MM, INTEGRAL, 3.25
FDA Adverse Event
Injury
·SULZER CALCITEK·Product code DZE·August 4, 1998
ABUTMENT: SHOULDERED, 2MM, INTEGRAL, 3.25
FDA Adverse Event
Injury
·SULZER CALCITEK·Product code DZE·August 4, 1998
IMPLANT: HA, 13MM, INTEGRAL, 3.25
FDA Adverse Event
Injury
·SULZER CALCITEK·Product code DZE·November 11, 1997
IMPLANT: HA, 13MM, INTEGRAL OMNLIOC, 3.25
FDA Adverse Event
Injury
·SULZER CALCITEK INC.·Product code DZE·June 5, 1997
IMPLANT: HA, 13MM, INTEGRAL, 3.25
FDA Adverse Event
Injury
·SULZER CALCITEK·Product code DZE·March 11, 1998
IMPLANT: HA, 15MM, INTERGAL OMNILOC, 3.25
FDA Adverse Event
Injury
·SULZER CALCITEK INC.·Product code DZE·June 5, 1997
IMPLANT: HA,13MM, INTEGRAL OMNILOC, 3.25
FDA Adverse Event
Injury
·SULZER CALCITEK INC.·Product code DZE·June 5, 1997
IMPLANT: HA,10MM,INTEGRAL 3.5
FDA Adverse Event
Injury
·CALCITEK·Product code DZE·October 17, 1996