7 results
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18ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INTERPLEURAL ANESTHESIA CATHETER
FDA 510(k)
FDA Class 2
·Anesthesiology
SOFTXIL
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
HDC STERILE SPIDER SCREW
FDA 510(k)
FDA Class 2
·Dental
SUPERDIMENSION INREACH SYSTEM
FDA Adverse Event
Malfunction
·SUPERDIMENSION INC.·Product code JAK·February 15, 2013
PRECISION XTRA
FDA Adverse Event
Malfunction
·Product code NBW·January 27, 2011
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·July 31, 2014
RENEGADE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORK·Product code DQO·April 2, 2007