10 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Passeo-35 Xeo Peripheral Dilatation Catheter; Passeo-18 Peripheral Dilatation Catheters; Passeo-14 Peripheral Dilatation Catheter; Oscar Peripheral Multifunctional Catheter System; Pantera Pro Percutaneous Transluminal Coronary Angioplasty Catheter; Pantera LEO Percutaneous Transluminal Coronary Angioplasty (PTCA) Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
Ceramco® iC
FDA UDI
Dentsply International Inc.·D00142507060·
TIGERSHARK
FDA UDI
Choice Spine, LP·00840996185707·TIGER SHARK THTL,TRIAL 25X7X6DEGREE
VitalBeam
FDA 510(k)
FDA Class 2
·Radiology
HARMONY PORT SYSTEM, MODEL 1907 SERIES
FDA 510(k)
FDA Class 2
·Neurology
MAXPLUS POSITIVE PRESSURE CONNECTOR
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·May 29, 2019
TELEGRAPH®
FDA UDI
FOURNITURES HOSPITALIERES INDUSTRIE·03661489507069·
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·November 26, 2008
UNKNOWN DEEP BRAIN STIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·September 12, 2011
FEMTO LDV
FDA Adverse Event
Injury
·SIE AG, SURGICAL INSTRUMENT ENGINEERING·Product code GEX·July 19, 2013