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

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JUD custom fit condom

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

OsteoMed

FDA UDI
OSTEOMED LLC·00845694027175·2.4mm X 14mm Cannulated Headless Screw

OsteoMed

FDA UDI
OSTEOMED LLC·00845694068826·Cannulated 2.4 x 14mm Headless Screw Sterile Qty 5

CRYOSTAT

FDA 510(k)
FDA Unclassified ·Unknown

ELIA B2-GLYCOPROTEIN I IGA IMMUNOASSAY

FDA 510(k)
FDA Class 2 ·Immunology

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

COBAS E411 RACK SYSTEM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JLW·August 8, 2013

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

FREESTYLE

FDA Adverse Event
Malfunction ·Product code NBW·July 31, 2012

SCRW,2.4X8MM CANCELOUS LOCKING

FDA Adverse Event
Injury ·BIOMET MICROFIXATION·Product code HRS·June 17, 2013

PRECISION®

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 22, 2011

HS III PROXIMAL SEAL SYSTEM 3.8 MM

FDA Adverse Event
Injury ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·October 10, 2014