190 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NIOX VERO AIRWAY INFLAMMATION MONITOR
FDA 510(k)
FDA Class 2
·Clinical Toxicology
A SERIES AND Q SERIES PATIENT MONITORS
FDA 510(k)
FDA Class 2
·Cardiovascular
VOLCANO S5/S5I INTRAVASCULAR ULTRASOUND IMAGING AND PRESSURE SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
OPTILENE 3/0 (2) 90CM 2XHR26 CV RCP
FDA Adverse Event
Malfunction
·B. BRAUN SURGICAL, S.A.·Product code GAW·April 28, 2026
OPTILENE 6/0 (0,7) 75CM 2XDR13 CV2 RCP
FDA Adverse Event
Malfunction
·B. BRAUN SURGICAL, S.A.·Product code GAW·March 17, 2026
SPRINT QUATTRO SECURE
FDA Adverse Event
Death
·MPRI·Product code NVY·October 2, 2014
AEQUALIS
FDA Adverse Event
Injury
·TORNIER SAS·Product code KWS·May 23, 2013
R SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·May 12, 2011
OPTILENE 6/0 (0,7)75CM 2XPRC13B CV2 RCP
FDA Adverse Event
Malfunction
·B. BRAUN SURGICAL, S.A.·Product code GAW·March 25, 2026
CARDIOHELP
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·April 29, 2026
CARDIOHELP
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·April 8, 2026
CARDIOHELP
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·March 11, 2026
CARDIOHELP
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·May 26, 2026
OPTILENE 8/0 (0,4) 60CM 2XDR6 CV2 RCP
FDA Adverse Event
Malfunction
·B. BRAUN SURGICAL, S.A.·Product code GAW·January 28, 2026
OPTILENE 8/0 (0,4) 60CM 2XDR6 CV2 RCP
FDA Adverse Event
Malfunction
·B. BRAUN SURGICAL, S.A.·Product code GAW·January 28, 2026
OPTILENE 8/0 (0,4) 60CM 2XDR6 CV2 RCP
FDA Adverse Event
Malfunction
·B. BRAUN SURGICAL, S.A.·Product code GAW·January 28, 2026
CARDIOHELP
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·March 5, 2026
CARDIOHELP
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·May 19, 2026
CARDIOHELP
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·May 19, 2026
CARDIOHELP
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·May 18, 2026