51 results · 21ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

INVIROSTRIPE LUER LOCK SYRINGES (1, 3, 10, 20, 30 AND 60 ML)

FDA 510(k)
FDA Class 2 ·General Hospital

Preci-Sagix

FDA UDI
Preat Corporation·00842092108802·Sagix 2.2 Complete Metal

ILIZAROV

FDA UDI
Smith & Nephew, Inc.·03596010030511·HALF RING 220MM COMPOSITE

JOBST Bella Lite

FDA UDI
BSN MEDICAL, INC.·00035664013592·BELLA LITE 20-30 MM HG GAUNTLET MEDIUM BLACK 1 ...

Multi-Purpose Workstation ™ Stepper

FDA UDI
CIVCO MEDICAL INSTRUMENTS CO., INC.·00841436114301·For use with Exact Imaging EV29L transducers

MED-RX

FDA UDI
Canadian Hospital Specialties Limited·00628725024967·MED-RX Insufflation Filter Set

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172973271·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172971178·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172972991·

MODIFICATION TO KSEA ENDOTIP SYSTEM

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

DASH 3000/4000 PATIENT MONITOR

FDA 510(k)
FDA Class 2 ·Cardiovascular

CareLiving Blood Lancet 310pcs Multi-Color

FDA UDI
Care Living Diagnostics Inc.·00383568101359·• 30 Gauge • Multi-Color•Twist top lancets • Si...

Recon

FDA UDI
Revelation Medical Devices·G31810135910·Richardson Retractor

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