34 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Terumo Capiox FX15 Advance Oxygenator with Integrated Arterial Filter and Hardshell Reservoir
FDA 510(k)
FDA Class 2
·Cardiovascular
ProLift Trial
FDA UDI
Life Spine, Inc.·00190837087333·
SAPPHIRE INFUSION PUMP
FDA 510(k)
FDA Class 2
·General Hospital
JUSHA-C31 MEDICAL DISPLAY
FDA 510(k)
FDA Class 2
·Radiology
ROSA ONE
FDA Adverse Event
Injury
·MEDTECH SA·Product code HAW·November 10, 2017
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·April 11, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·March 15, 2018
ROSA ONE
FDA Adverse Event
Injury
·MEDTECH SA·Product code HAW·June 15, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·November 10, 2017
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·March 21, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·November 16, 2017
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·November 9, 2017
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·January 26, 2018
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 30, 2013
LIFEPAK 12 DEFIBRILLATOR/MONITOR SERIES
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·June 8, 2011
SELOX ST 53
FDA Adverse Event
Injury
·BIOTRONIK GMBH AND CO.·Product code DTB·September 4, 2008
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·November 6, 2017
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·August 3, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·January 10, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·November 16, 2017