308 results · 30ms · Sources: EU EUDAMED, 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