39 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.

VISIGLIDE GUIDEWIRE

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·November 8, 2021

VISIGLIDE GUIDEWIRE

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·November 8, 2021

SINGLE USE REPOSITIONABLE CLIP

FDA Adverse Event
Injury ·AOMORI OLYMPUS CO., LTD.·Product code PKL·March 9, 2023

SINGLE USE REPOSITIONABLE CLIP

FDA Adverse Event
Injury ·AOMORI OLYMPUS CO., LTD.·Product code PKL·March 9, 2023

SINGLE USE REPOSITIONABLE CLIP

FDA Adverse Event
Injury ·AOMORI OLYMPUS CO., LTD.·Product code PKL·March 9, 2023

SINGLE USE REPOSITIONABLE CLIP

FDA Adverse Event
Injury ·AOMORI OLYMPUS CO., LTD.·Product code PKL·March 10, 2023

SINGLE USE REPOSITIONABLE CLIP

FDA Adverse Event
Injury ·AOMORI OLYMPUS CO., LTD.·Product code PKL·March 10, 2023

SINGLE USE REPOSITIONABLE CLIP

FDA Adverse Event
Injury ·AOMORI OLYMPUS CO., LTD.·Product code PKL·March 10, 2023

COTILO PRESSFIT-HAK CEDIOR 48

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·November 14, 2014

SINGLE USE ROTATABLE CLIP FIXING DEVICE

FDA Adverse Event
Injury ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code GDO·March 21, 2012

DRIVE

FDA Adverse Event
Injury ·LERADO H.K. LTD.·Product code INI·May 8, 2023

DRIVE DEVILBISS HEALTHCARE

FDA Adverse Event
Injury ·LERADO H.K. LIMITED·Product code INI·February 22, 2024

DRIVE

FDA Adverse Event
Injury ·LERADO H.K. LTD.·Product code INI·October 10, 2022

DRIVE

FDA Adverse Event
Injury ·LERADO H.K. LTD.·Product code INI·October 10, 2022

DRIVE

FDA Adverse Event
Injury ·LERADO H.K. LTD.·Product code INI·October 10, 2022

OLYMPUS SIGNLE USE ROTATABLE CLIP FIXING DEVICE

FDA Adverse Event
Injury ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code GDO·March 14, 2012

SINGLE USE RETRIEVAL BASKET V

FDA Adverse Event
Injury ·AOMORI OLYMPUS CO., LTD.·Product code LQR·February 28, 2024

HOFF PASS-LONG

FDA Adverse Event
Injury ·CODMAN & SHURTLEFF·Product code GYK·May 15, 2014

CODMAN BACTISEAL VENTRICULAR CATHETER

FDA Adverse Event
Injury ·CODMAN & SHURTLEFF, INC.·Product code GYK·May 12, 2014

FEMALE FOLEY ADAPTER

FDA Adverse Event
Injury ·COOK INCORPORATED·Product code EYK·June 6, 2024