190 results · 27ms · Sources: EU EUDAMED, 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