34 results · 21ms · Sources: EU EUDAMED, 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