6,480 results · 33ms · Sources: EU EUDAMED, US FDA

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Jay Adjustable Solid Seat

FDA UDI
SUNRISE MEDICAL (US) LLC·00016958040128·The Adjustable Solid Seat features ABS plastic ...

MONITOR DEFIBRILLATOR GPN

FDA Adverse Event
Death ·HEWLETT PACKARD·Product code DRK·July 13, 1993

FILIFORM DOUBLE PIGTAIL URETERAL STENT SET

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·May 22, 2023

SINGLE LUMEN POLYETHYLENE CENTRAL VENOUS CATHETER TRAY

FDA Adverse Event
Malfunction ·COOK INC·Product code FOZ·May 20, 2019

ACT ARTIC HD ARCOM XL 28X46MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWY·November 19, 2018

DELTA CERAMIC OPTION HEAD DIA2 8

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LZO·November 19, 2018

G7 PPS LTD ACET SHELL 58G

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code PBI·October 10, 2018

DELTA CERAMIC FEMORAL HEAD Ø32/ 0MM T1

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code LZO·March 2, 2017

UNKNOWN

FDA Adverse Event
Injury ·COOK INC·Product code DYB·May 3, 2018

EVOLUTION DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code MUM·September 9, 2019

SAFE-T-J ROSEN CATHETER EXCHANGE WIRE GUIDE

FDA Adverse Event
Malfunction ·COOK INC·Product code DQY·December 13, 2017

UNKNOWN

FDA Adverse Event
Injury ·COOK INC·Product code DYG·May 8, 2018

UNKNOWN

FDA Adverse Event
Injury ·COOK INC·Product code DXE·May 9, 2018

COOK CELECT PLATINUM NAVALIGN FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·August 13, 2020

FLEXOR ANSEL GUIDING SHEATH

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·November 20, 2017

STENT, CORONARY

FDA Adverse Event
Death ·COOK INC·Product code MAF·June 9, 2022

UNKNOWN

FDA Adverse Event
Malfunction ·Product code LIT·October 29, 2018

STENT, CORONARY

FDA Adverse Event
Injury ·COOK INC·Product code MAF·June 9, 2022

BEACON TIP TORCON NB ADVANTAGE ANGIOGRAPHIC CATHETER

FDA Adverse Event
Death ·COOK INC·Product code DQO·April 8, 2020

1820334-2019-01090

FDA Adverse Event
Injury ·COOK INC·Product code BTR·May 16, 2019