1,262 results · 28ms · Sources: EU EUDAMED, US FDA

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STRYKER SILVERGLIDE BIPOLAR FORCEPS REUSABLE CABLE; DISPOSABLE CABLE

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587X0618350·6mm H x 18mm W x 35mm L x 0 degrees XLIF

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587X06183580·6mm H x 18mm W x 30mm L x 8 degrees XLIF

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587X061835120·6mm H x 18mm W x 35mm L x 12 degrees XLIF

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587L061835120·6mm H x 18mm W x 35mm L XLIF Trial 12 degree Lo...

Specials

FDA UDI
Seaspine Orthopedics Corporation·10889981276058·Ø3.5mm DRILL, CANNULATED, A/O

IRV2000 INDIVIDUAL RECREATIONAL VEHICLE

FDA 510(k)
FDA Class 2 ·Physical Medicine

COBE REVOLUTION

FDA 510(k)
FDA Class 2 ·Cardiovascular

TRIMA ACCEL

FDA Adverse Event
Malfunction ·TERUMO BCT·Product code GKT·April 16, 2013

UNIFY ASSURA DR CRT-D

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·September 4, 2014

RESTORE RECHARGABLE NEUROSTIMULATOR

FDA Adverse Event
Malfunction ·MDTPUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·April 4, 2011

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·August 14, 2015

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·October 26, 2016

UNKNOWN

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DTK·March 10, 2016

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·January 5, 2017

COOK CELECT JUGULAR VENA CAVA FILTER SET

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DTK·August 14, 2015

COOK CELECT FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·December 15, 2015

UNKNOWN

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DTK·December 15, 2015

UNKNOWN

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DTK·November 19, 2015

UNKNOWN

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DTK·December 15, 2015