29 results · 23ms · Sources: EU EUDAMED, US FDA

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POWDER FREE NITRILE EXAMINATION GLOVE-BLUE (CHEMOTHERAPY)

FDA 510(k)
FDA Class 1 ·General Hospital

NEODYNE DRESSING

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

NANO-CHECK AMI CTNI CARDIAC MARKER TEST

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

ZENIX

FDA UDI
Zoll Medical Corporation·00198843000070·ZENIX, EMS CRITICAL CARE CONFIGURATION

UNKNOWN DEEP BRAIN STIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 16, 2010

UNKNOWN DEEP BRAIN STIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 16, 2010

UNKNOWN DEEP BRAIN STIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 16, 2010

UNKNOWN DEEP BRAIN STIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 16, 2010

UNKNOWN DEEP BRAIN STIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 16, 2010

UNKNOWN DEEP BRAIN STIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 16, 2010

UNKNOWN DEEP BRAIN STIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 16, 2010

UNKNOWN DEEP BRAIN STIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 16, 2010

UNK DEEP BRAIN STIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 16, 2010

UNKNOWN DEEP BRAIN STIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 16, 2010

UNK DEEP BRAIN STIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 16, 2010

UNKNOWN DEEP BRAIN STIMULATOR

FDA Adverse Event
Death ·MEDTRONIC NEUROMODULATION·Product code MHY·April 16, 2010

AVAULTA PLUS BIOSYNTHETIC SUPPORT SYSTEM - ANTERIOR

FDA Adverse Event
Injury ·C.R. BARD, INC. (COVINGTON)·Product code OTP·May 17, 2013

HEARTSTART FR3, ECG, BASIC BUNDLE, JAPAN

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·September 19, 2014

STAR TOTAL ANKLE REPLACEMENT

FDA Adverse Event
Injury ·WALDEMAR LINK, GMBH & CO·Product code HSN·June 3, 2011

IMPLANTABLE LEAD

FDA Adverse Event
Product code OJX·May 7, 2010