12 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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T:CONNECT DATA MANAGEMENT SYSTEM
FDA 510(k)
FDA Class 1
·General Hospital
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973516·
ZIP'R4/ ZIP'R4 XTRA SCOOTER
FDA 510(k)
FDA Class 2
·Physical Medicine
ALAMO C
FDA 510(k)
FDA Class 2
·Orthopedic
CUSA EXCEL 23KHZ STANDARD TIP
FDA Adverse Event
Malfunction
·INTEGRA LIFESCIENCES (IRELAND) LIMITED·Product code LFL·September 10, 2013
CUSA EXCEL 23KHZ STANDARDTIP
FDA Adverse Event
Malfunction
·INTEGRA LIFESCIENCES (IRELAND) LIMITED·Product code LBK·September 10, 2013
MULTI-LINK 8
FDA Adverse Event
Death
·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code MAF·October 19, 2010
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·May 21, 2013
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Injury
·ANIMAS CORPORATION·Product code LZG·June 13, 2011
OMNIPOD INSULIN PUMP
FDA Adverse Event
Other
·INSULET CORPORATION·Product code LZG·August 15, 2008
INTELLAMAP ORION¿
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code DRF·February 18, 2016
MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER, featuring IsoSilk(R), 13cm x 244 cm, 5" x 96", REF PC3688N, QTY 100, Microtek Medical, Inc., Columbus, MS 39702.
FDA Enforcement
Class II
·Terminated·Ecolab Inc·February 19, 2014