10,000 results · 53ms · Sources: EU EUDAMED, US FDA

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ARCTIC FRONT ADVANCE PRO

FDA Adverse Event
Malfunction ·MEDTRONIC, INC.·Product code OAE·March 10, 2021

COSGROVE-EDWARDS ANNULOPLASTY SYSTEM

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code KRH·September 1, 2004

S3 DOUBLE HEAD PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DWB·May 2, 2014

ALLURA XPER FD10/10

FDA Adverse Event
Malfunction ·PHILIPS HEALTHCARE·Product code IZI·August 24, 2011

PLATINIUM

FDA Adverse Event
Malfunction ·MICROPORT CRM S.R.L.·Product code LWS·January 20, 2025

BV 25 GOLD 9"

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code IZL·October 20, 2010

REDIGUARD IAB CATHETER

FDA Adverse Event
Malfunction ·BARD VASCULAR SYSTEM·Product code DSP·October 24, 1996

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 10, 2011

PLATINIUM

FDA Adverse Event
Malfunction ·MICROPORT CRM S.R.L.·Product code NIK·September 9, 2025

T:FLEX INSULIN DELIVERY SYSTEM

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code LZG·December 19, 2019

MEDTRONIC LEAD

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code DXY·October 6, 2017

IVENT 201

FDA Adverse Event
Malfunction ·VERSAMED MEDICAL SYSTEMS LTD.·Product code CBK·February 3, 2011

ULYS

FDA Adverse Event
Injury ·MICROPORT CRM S.R.L.·Product code MRM·July 1, 2024

E-LUMINEXX VASCULAR STENT

FDA Adverse Event
Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK·Product code NIO·March 22, 2011

CORE SUMEX DRILL

FDA Adverse Event
Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code DZJ·July 27, 2012

DRILL, AO, STERILE 4,2X180 MM

FDA Adverse Event
Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HBE·December 16, 2010

5F STIFF MICRO STICK

FDA Adverse Event
Injury ·MEDCOMP·Product code DQX·May 2, 2014

12.5FX28CM HEMO-CATH

FDA Adverse Event
Malfunction ·MEDCOMP·Product code MSD·September 20, 2013

12.5FX28CM PC HEMO-CATH

FDA Adverse Event
Malfunction ·MEDCOMP·Product code MSD·September 20, 2013

ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION CORPORATION·Product code FRN·August 31, 2011