28 results · 24ms · 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.

ANATOMIC PEEK CERVICAL FUSION SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

ABN ANEROID SPHYGMOMANOMETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

POWDER-FREE VINYL PATIENT EXAMINATION GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

ROSA ONE

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

ROSA ONE

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

ROSA ONE

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

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code HAW·October 17, 2018

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code HAW·November 9, 2018

ROSA ONE

FDA Adverse Event
Injury ·MEDTECH SA·Product code HAW·January 11, 2019

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code NAY·January 21, 2019

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code HAW·December 21, 2018

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code OLO·November 15, 2018

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code OLO·November 15, 2018

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·May 14, 2013

BRIGHTVIEW GAMMA CAMERA SYSTEM

FDA Adverse Event
PHILIPS MEDICAL SYSTEMS (CLEVELAND), INC.·Product code KPS·March 23, 2011

VERSACARE

FDA Adverse Event
Malfunction ·HILL-ROM RITTER·Product code FNL·August 15, 2008

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code OLO·November 15, 2018

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·June 6, 2018

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code OLO·October 22, 2018