38 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LIGAFIX RESORBABLE INTERFERENCE SCREW, MODELS 30 AND 60
FDA 510(k)
FDA Class 2
·Orthopedic
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526768512·GENUMEDI PSS GREEN VII
LORENZ BLUE DEVICE
FDA 510(k)
FDA Class 2
·Dental
ADVISOR, MODEL 9200
FDA 510(k)
FDA Class 2
·Anesthesiology
MARY HITCHCOCK HANOVER NH 1
FDA Adverse Event
Other
·SORIN GROUP ITALIA·Product code DTZ·November 7, 2012
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
DIDECO COMPACTFLO EVO
FDA Adverse Event
Other
·SORIN GROUP ITALIA·Product code DTZ·October 8, 2013
LIBERTY CYCLER SET, DUAL PT CONNECT
FDA Adverse Event
Malfunction
·REYNOSA MANUFACTURING·Product code FKX·April 8, 2013
TENDRIL DX
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·May 27, 2008
ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·April 5, 2011
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