1,253 results · 38ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

530G INSULIN PUMP

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·December 30, 2015

UTQ 200CM BWF 2HK2F CHSO 10PK

FDA Adverse Event
Injury ·A&E MEDICAL CORPORATION·Product code LDF·July 7, 2025

UTQ 200CM BWF 2HK2F CHSO 10PK

FDA Adverse Event
Injury ·A&E MEDICAL CORPORATION·Product code LDF·July 7, 2025

UTQ 200CM BWF 2HK2F CHSO 10PK

FDA Adverse Event
Injury ·A&E MEDICAL CORPORATION·Product code LDF·July 7, 2025

DWF CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS

FDA Adverse Event
Injury ·COOK VASCULAR INC·Product code DWF·December 15, 2016

AVIATOR VARIABLE SELF DRILLING SCREW 4X12MM

FDA Adverse Event
Injury ·STRYKER SPINE BORDEAUX·Product code KWQ·February 6, 2012

ZIRALLOY CERAMIC FEMORAL HEAD, BIOPRO

FDA Adverse Event
Injury ·BIOPRO, CIV IF IMT·Product code KWY·January 27, 1997

UNI 2 IMPLANT SET

FDA Adverse Event
Injury ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code JWJ·April 12, 2016

S-ROM M HEAD 36MM +0

FDA Adverse Event
Injury ·IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE·Product code LPH·December 26, 2012

LCS COMP RP INSERT LG+ 10MM

FDA Adverse Event
Injury ·DEPUY-RAYNHAM, A DIVISION IF DEPUY ORTHOPAEDICS, INC.·Product code NJL·May 29, 2009

VITAL-PORT DETACHED SILICONE CATHETER TITANIUM INFUSION PORT

FDA Adverse Event
Injury ·COOK VASCULAR INC·Product code DWF·December 14, 2016

EOPA ARTERIAL CANNULA

FDA Adverse Event
Injury ·MEDTRONIC PERFUSION SYSTEMS·Product code DWF·December 21, 2016

AORTIC PERFUSION CANNULA

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code DWF·December 12, 2016

HLM TUBING SET W/SOFTLINE COATING

FDA Adverse Event
Injury ·MAQUET CARDIOPULMONARY AG·Product code DWF·July 20, 2015

CLEARVIEW ARTERIOTOMY SHUNT

FDA Adverse Event
Injury ·PERFUSION SYSTEMS·Product code DWF·September 18, 2015

BE-HLS CANNULA 23F VL

FDA Adverse Event
Injury ·MAQUET CARDIOPULMONARY AG·Product code DWF·July 7, 2015

10023# AVALON ELITE 23F, 31CM

FDA Adverse Event
Injury ·MAQUET CARDIOPULMONARY AG·Product code DWF·August 7, 2015

AVALON ELITE BI-CAVAL DUAL LUMEN CATHETER

FDA Adverse Event
Injury ·AVALON LABORATORIES, LLC.·Product code DWF·March 30, 2012

RETROPLEGIA/CARDIOPLEGIA CANNULA

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code DWF·February 7, 2012

VITAL-PORT DETACHED SILICONE CATHETER TITANIUM INFUSION PORT

FDA Adverse Event
Injury ·COOK VASCULAR INC.·Product code DWF·January 5, 2012