30 results · 24ms · Sources: EU EUDAMED, US FDA

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SONON Ultrasound Imaging System (Model: SONON 300C)

FDA 510(k)
FDA Class 2 ·Radiology

R&D CBC-4K PLUS RETICS HEMATOLOGY CONTROL

FDA 510(k)
FDA Class 2 ·Hematology

ARCHER SUPER STIFF GUIDEWIRES

FDA 510(k)
FDA Class 2 ·Cardiovascular

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

KAPPA 900 SR

FDA Adverse Event
Death ·IPG MFG SWITZERLAND·Product code DXY·June 7, 2013

UNKNOWN DEPUY ASR HIP

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 30, 2011

POWERED WHEELCHAIR

FDA Adverse Event
Malfunction ·INVACARE TAYLOR STREET·Product code ITI·October 8, 2014

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

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code HAW·June 6, 2018