836 results · 27ms · Sources: EU EUDAMED, US FDA

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SAFETY SYRINGE

FDA 510(k)
FDA Class 2 ·General Hospital

Arx

FDA UDI
Life Spine, Inc.·00190837172589·

ARx SAI

FDA UDI
Life Spine, Inc.·00190837194536·

YASARGIL PERMANENT ANEURYSM CLIPS

FDA 510(k)
FDA Class 2 ·Neurology

SIMPLE

FDA 510(k)
FDA Class 2 ·Dental

ANIMAS INSULIN CARTRIDGE

FDA Adverse Event
Injury ·ANIMAS CORPORATION·Product code LZG·April 11, 2013

HEARTSTART MRX-EMS DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code LDD·May 28, 2008

ADAPTA DR

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL, INC.·Product code NVZ·April 13, 2011

EGIA ULTRA UNIVERSAL SHORT STAPLER

FDA Adverse Event
Injury ·COVIDIEN, FORMERLY US SUR·Product code GDW·April 18, 2012

ENDO GIA ROTICULATOR* 60-3.5 SULU

FDA Adverse Event
Injury ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GDW·October 10, 2014

IDRIVE ULTRA POWERED HANDLE 1

FDA Adverse Event
Malfunction ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GDW·September 19, 2016

ENDO GIA* II 45-2.5 DLU

FDA Adverse Event
Injury ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GAG·October 9, 2014

OT ULTRA2 METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·March 26, 2012

OT ULTRA2 METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·December 13, 2010

OT ULTRA2 METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·December 7, 2010

OT ULTRA2 METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·February 16, 2011

OT ULTRA2 METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·February 23, 2011

OT ULTRA2 METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·February 28, 2011

ENDO GIA ROTICULATOR* 60-4.8 SULU

FDA Adverse Event
Injury ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GDW·November 25, 2014

OT ULTRA2 METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·March 27, 2012