110 results · 40ms · 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.

RADIFOCUS GLIDEWIRE M

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·January 22, 2018

SPRINT QUATTRO

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code LWS·December 13, 2010

DIMENSION XPAND PLUS WITH HM

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code JJE·July 9, 2014

AFFINITY THREE BIRTHING BED

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code HDD·December 27, 2012

RADIFOCUS GLIDEWIRE

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·December 29, 2025

RADIFOCUS GLIDEWIRE

FDA Adverse Event
Injury ·TERUMO MEDICAL CORPORATION·Product code DQX·May 16, 2024

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 21, 2021

RADIFOCUS GLIDEWIRE

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·October 6, 2025

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Injury ·TERUMO MEDICAL CORPORATION·Product code DQX·September 15, 2023

GUIDE WIRE M

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 25, 2025

RADIFOCUS GUIDEWIRE

FDA Adverse Event
Injury ·TERUMO MEDICAL CORPORATION·Product code DQX·December 5, 2023

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·April 3, 2018

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·January 23, 2026

RADIFOCUS GLIDEWIRE

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·March 11, 2026

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·April 12, 2021

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 22, 2021

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 20, 2021

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·April 20, 2022

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·April 24, 2022

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·November 17, 2021