1,109 results · 27ms · Sources: EU EUDAMED, US FDA

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CD HORIZON™ Spinal System

FDA 510(k)
FDA Class 2 ·Orthopedic

Modular Evolve Stem Pusher

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215055592·

APLIO XG DIAGNOSTIC ULTRASOUND SYSTEM, MODEL SSA - 790A VERSION 3.0

FDA 510(k)
FDA Class 2 ·Radiology

SUR-G GLOV AND MAXITEX

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

GUNTHER TULIP JUGULAR VENA CAVA FILTER SET

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

POWERED WHEELCHAIR

FDA Adverse Event
Malfunction ·INVACARE TAYLOR STREET·Product code ITI·October 17, 2014

S3 EX - 3005

FDA Adverse Event
Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·June 21, 2013

R SERIES DEFIBRILLATOR

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·June 23, 2011

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·May 20, 2016

UNKNOWN

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

UNKNOWN

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

GUNTHER TULIP JUGULAR & FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·February 9, 2017

GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·June 3, 2016

UNKNOWN

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

GUNTHER TULIP JUGULAR VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·November 8, 2016

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·December 21, 2016

GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·November 15, 2016

GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·February 25, 2016

GUNTHER TULIP JUGULAR VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·September 29, 2016

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·July 18, 2016