1,914 results
·
21ms
·
Sources: EU EUDAMED, US FDA
SKIN CLOSURE TAPES STERILE
FDA 510(k)
FDA Class 1
·General Hospital
ReLine
FDA UDI
Nuvasive, Inc.·00887517010711·RELINE-C Tap, 4.0mm Single Lead
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515204195·Pliers, Parallel, max open 1/2", 7"
discovery®
FDA UDI
DENTAURUM GmbH & Co.KG·J011790140000·discovery® Bracket, - 14° Torque, 0° Angulation...
GUNTHER TULIP VENA CAVA FILTER, COOK CELECT VENA CAVA FILTER
FDA 510(k)
FDA Class 2
·Cardiovascular
BANDAGE, WRINKY-LASTIC ELASTIC GAUZE
FDA 510(k)
FDA Class 1
·General Hospital
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·May 5, 2014
EXTERNAL PULSE GENERATOR
FDA Adverse Event
Malfunction
·MEDTRONIC MILACA INC.·Product code DTE·October 15, 2012
SCORPIO M-DOME PATELLA
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·August 3, 2010
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
Injury
·WILLIAM COOK EUROPE·Product code DTK·October 26, 2016
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
COOK CELECT JUGULAR VENA CAVA FILTER SET
FDA Adverse Event
Malfunction
·WILLIAM COOK EUROPE·Product code DTK·August 14, 2015
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