9 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
FUSION VASCULAR GRAFT AND FUSION BIOLINE VASCULAR GRAFT
FDA 510(k)
FDA Class 2
·Cardiovascular
FUSION 8MM-40CM UNSUPP PERIPHERAL GRAFT
FDA Adverse Event
Malfunction
·MAQUET CV·Product code DSY·February 8, 2017
Oticon
FDA UDI
Oticon A/S·05707131256423·NERA, BTE 13 WL 85 TC
PRACTICEBUILDER 1-2-3
FDA 510(k)
FDA Class 2
·Radiology
GIRAFFE INCUBATOR
FDA 510(k)
FDA Class 2
·General Hospital
CANTATA 2.9 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·September 14, 2017
TELIGEN
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 1, 2014
SPRINT QUATTRO
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·June 16, 2011
STEALTHSTATION TREON TREATMENT GUIDANCE SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·May 29, 2013