4 results
·
29ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
CA-1000
FDA Adverse Event
Injury
·TOA MEDICAL ELECTRONICS·Product code GKP·January 6, 1997
E360 VENTILATOR
FDA Adverse Event
Malfunction
·NEWPORT MEDICAL INSTRUMENTS·Product code CBK·January 4, 2013
MEDISENSE OPTIUM
FDA Adverse Event
Malfunction
·Product code NBW·December 21, 2010
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code FRN·February 4, 2014