3,278 results · 23ms · Sources: EU EUDAMED, US FDA

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ULTIMA SIZE 0 CEMENTED FEMORAL STEM

FDA 510(k)
FDA Class 2 ·Orthopedic

APEX Knee System

FDA UDI
Omni Life Science, Inc.·00841690196600·Revision Knee Spiral Reamer- Hudson Short Flute...

Medtronic Vascular

FDA registration
Medtronic Vascular·10 products·🇺🇸 United States

VALIANT THORACIC STENT GRAFT SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code MIH·August 15, 2011

VALIANT THORACIC STENT GRAFT SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code MIH·August 15, 2011

VALIANT THORACIC STENT GRAFT SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code MIH·August 15, 2011

SnoreRx

FDA 510(k)
FDA Class 2 ·Dental

GORE SEAMGUARD STAPLE LINE REINFORCEMENT MATERIAL

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

2953200-2018-01139

FDA Adverse Event
Injury ·August 7, 2018

2953200-2018-01130

FDA Adverse Event
Malfunction ·August 3, 2018

LAUNCHER 7F (EBU3.75)

FDA Adverse Event
Death ·MEDTRONIC INC.·Product code DQY·May 20, 2010

TALENT CAPTIVIA STENT GRAFT

FDA Adverse Event
Death ·MEDTRONIC CARDIOVASCULAR IRELAND·Product code MIH·July 13, 2011

ACCU-CHEK ® COMFORT CURVE TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 18, 2010

ACCU-CHEK ® COMFORT CURVE TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 3, 2010

ACCU-CHEK ® COMFORT CURVE TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 18, 2010

ACCU-CHEK ® COMFORT CURVE TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 20, 2010

ACCU-CHEK ® COMFORT CURVE TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 18, 2010

ACCU-CHEK ® AVIVA TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 17, 2010

ACCU-CHEK ® COMFORT CURVE TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 20, 2010

TALENT THORACIC STENT GRAFT WITH XCELERANT

FDA Adverse Event
Death ·MEDTRONIC CARDIOVASCULAR·Product code MIH·July 13, 2011