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