7 results
·
26ms
·
Sources: EU EUDAMED, US FDA
COBE OPTIMIN HOLLOW FIBER MEMBRANE OXYGENATOR
FDA 510(k)
FDA Class 2
·Cardiovascular
FORE-SIGHT, MODEL MC-2000 SERIES (MC 2000, MC2010, MC-2020,MC2030)
FDA 510(k)
FDA Class 2
·Cardiovascular
AGGLUTINOTEST-TUBERCULOSIS
FDA 510(k)
FDA Class 1
·Microbiology
INVISION-PLUS
FDA Adverse Event
Malfunction
·RYMED TECHNOLOGIES, LLC·Product code FPA·July 7, 2022
PROGRAMMABLE VALVE INLINE
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC.·Product code JXG·March 6, 2013
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MPRI·Product code DTB·August 8, 2014
REVEAL XT
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code DSI·February 15, 2011