1,949 results · 67ms · Sources: EU EUDAMED, US FDA

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C MEDICAL SUPPLIES

FDA registration
C MEDICAL SUPPLIES·2 products·🇨🇦 Canada

SYNCARDIA FREEDOM A/C POWER SUPPLY

FDA Adverse Event
Malfunction ·SYNCARDIA SYSTEMS, INC.·Product code LOZ·April 15, 2015

SYNCARDIA FREEDOM DRIVER

FDA Adverse Event
Malfunction ·SYNCARDIA SYSTEMS, INC.·Product code LOZ·April 15, 2015

T.W. POWER SUPPLY

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR LLC·Product code HQO·October 4, 2019

HEMOPRO POWER SUPPLY

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR LLC·Product code HQO·April 27, 2023

SYNCARDIA FREEDOM DRIVER

FDA Adverse Event
Malfunction ·SYNCARDIA SYSTEMS, INC.·Product code LOZ·January 29, 2015

FLUOROSCAN

FDA Adverse Event
Malfunction ·HOLOGIC, INC·Product code OXO·April 20, 2018

V60 VENTILATOR

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·August 15, 2019

HIGH FLOW INSUFFLATION UNIT

FDA Adverse Event
Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code HIF·August 3, 2021

VASOVIEW HEMOPRO

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR LLC·Product code GEI·December 13, 2023

REMSTAR PRO C-FLEX+

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·February 21, 2023

HEARTWARE HVAD CONTROLLER

FDA Adverse Event
Malfunction ·HEARTWARE INC / MEDTRONIC INC.·Product code DSQ·November 13, 2018

INTRALASE FS2

FDA Adverse Event
Malfunction ·ABBOTT MEDICAL OPTICS·Product code HNO·June 25, 2014

V60 VENTILATOR

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·July 22, 2019

COMMUNICATOR

FDA Adverse Event
Injury ·EXTERNAL MANUFACTURER·Product code LWS·April 13, 2011

ARCTIC SUN® 5000

FDA Adverse Event
Malfunction ·MEDIVANCE, INC. ¿ 1725056·Product code DWJ·May 25, 2021

HAMILTON-T1

FDA Adverse Event
Malfunction ·HAMILTON MEDICAL AG·Product code CBK·December 17, 2024

ESPRIT VENTILATOR

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code CBK·October 25, 2016

HAMILTON-T1

FDA Adverse Event
Malfunction ·HAMILTON MEDICAL AG·Product code CBK·November 7, 2024

PULSERA C-ARM

FDA Adverse Event
Other ·PHILIPS MEDICAL SYSTEMS·Product code JAK·October 1, 2010