7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
NP MEDICAL CAPLESS LUER ACTIVATED VALVE
FDA 510(k)
FDA Class 2
·General Hospital
Finapres Nova Noninvasive Hemodynamic Monitor
FDA 510(k)
FDA Class 2
·Cardiovascular
'E' CUBE AND 'E' PAD
FDA 510(k)
FDA Class 1
·Ophthalmic
CAPIOX HEMOCONCENTRATOR
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code KDI·March 3, 2016
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·February 22, 2013
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·August 1, 2014
PRECISION TEST STRIPS
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011