28 results
·
39ms
·
Sources: EU EUDAMED, US FDA
VEINNOVATIONS INFILTRATION SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
MAKRITE TYPE N95 RESPIRATOR AND SURGICAL MASK MODEL 910-N95
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
VIEW NT
FDA 510(k)
FDA Class 2
·Radiology
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·March 3, 2025
MADIGAN ARMY TACOMA WA 1
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code DWE·December 7, 2009
UNIV OF VA CHARLOTTESVILLE VA1
FDA Adverse Event
Other
·SORIN GROUP ITALIA·Product code DWF·December 28, 2010
HCSG MIDWEST REG LEXINGTON KY1
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code DWE·February 16, 2010
DIDECO COMPACTFLO EVO
FDA Adverse Event
Other
·SORIN GROUP USA ITALIA·Product code DTZ·November 27, 2012
PENROSE HSP CO SPRINGS CO 1
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code DTZ·April 4, 2007
UNIV OF VA CHARLOTTESVILLE VA1
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code DWE·April 20, 2011
WV UNIV HSP MORGANTOWN WV 1
FDA Adverse Event
Other
·SORIN GROUP USA·Product code DTZ·November 10, 2011
BASIS¿ SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC·Product code KWP·July 19, 2012
DIDECO COMPACTFLO EVO
FDA Adverse Event
Other
·SORIN GROUP ITALIA·Product code DTZ·October 8, 2013
PIPELINE EMBOLIZATION DEVICE
FDA Adverse Event
Injury
·EV3 NEUROVASCULAR·Product code OUT·April 10, 2013
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORP.·Product code LZG·April 5, 2011
TENDRIL SDX
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·May 27, 2008
UNIV OF CHARLOTTESVILLE VA1
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code DTZ·April 21, 2011
UNIV OF VA CHARLOTTESVILLE VA1
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code DWE·March 1, 2010
UNIV OF VA CHARLOTTESVILLE VA1
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code DWE·March 29, 2010
UNIV OF VA CHARLOTTESVILLE VA1
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code DWE·April 15, 2011