7 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OSTEONICS SERIES 7000 TOTAL KNEE FEMORAL COMPONENTS
FDA 510(k)
FDA Class 2
·Orthopedic
COPAL DIGITAL SPHYGMOMAMOMETER UA-550
FDA 510(k)
FDA Class 2
·Cardiovascular
MODEL 3500 MR-COMPATIBLE PULSE OXIMETER
FDA 510(k)
FDA Class 2
·Cardiovascular
APC PLUS, CLARITY, MINI UNI-TWIN, VICTORY SERIES
FDA Adverse Event
Injury
·3M UNITEK·Product code DYH·May 9, 2012
TOTALCARE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·January 10, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 6, 2010
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 18, 2014