7 results
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19ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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FDA 510(k)
FDA Class 2
·Radiology
MODIFICATION TO BD ECLIPSE HYPODERMIC NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
ACCUVIX XG DIAGNOSTIC ULTRASOUND SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
25 G X 5/8 IN. BD ECLIPSE¿ NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMI·March 1, 2016
FOGARTY ARTERIAL EMBOLECTOMY CATHETER
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES, PR·Product code DXE·June 3, 2013
OXYALERT NIRSENSOR INFANT
FDA Adverse Event
Injury
·COVIDIEN·Product code MUD·August 7, 2014
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·June 29, 2011