10 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
WAHL SPORTS RELIEF HOT/COLD MASSAGER ROLLER
FDA 510(k)
FDA Class 1
·Physical Medicine
THIGH AND FOOT POSITIONER, SUPRONE PLUS, MODEL RT-6010
FDA 510(k)
FDA Class 2
·Radiology
Evis Exera III Duodenovideoscope Olympus TJF-Q190V (TJF-Q190V)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
BD ANGIOCATH¿ IV CATHETER 22 G X 1"
FDA Adverse Event
Malfunction
·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·September 13, 2017
TANDEM T:SLIM INSULIN DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·TANDEM DIABETES·Product code LZG·June 9, 2014
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code FSA·February 8, 2013
NC QUANTUM APEX PTCA DILATATION CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·January 6, 2011
BD ANGIOCATH¿ IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FOZ·August 8, 2017
Pacemaker Kit, part number AMS4281 Pacemaker Kit, part number AMS4281(A Pacemaker Kit, part number AMS4281(C Pacemaker Kit, part number AMS4281(D
FDA Enforcement
Class II
·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017
Percutaneous Entry Kit, part number TVS4022(D Percutaneous Entry Kit , part number TVS4022(E Percutaneous Entry Kit, part number TVS4022(F
FDA Enforcement
Class II
·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017