27 results
·
27ms
·
Sources: EU EUDAMED, US FDA
BRACHYSEED PD-103 MODELS #PD1
FDA 510(k)
FDA Class 2
·Radiology
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040013878·Zirlux 16+ C1 98.5X18
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450217849·
MATIRA ANTERIOR CERVICAL SYSTEM
FDA UDI
Kalitec Direct LLC·B07307K0111101·AWL, 10MM SPRING LOADED
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033232583·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033232569·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033232606·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033232613·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033232576·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033232590·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033232620·
M2A ACETABULAR SYSTEM
FDA 510(k)
FDA Class 3
·Orthopedic
ROVERS ENDOCERVEX-BRUSH
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
GRANUFLO
FDA Adverse Event
Injury
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·March 15, 2013
MEDISENSE OPTIUM
FDA Adverse Event
Malfunction
·Product code NBW·March 8, 2011
VICTORY XL DR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·March 10, 2008
UNKNOWN_PUMP
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·April 25, 2014
UNKNOWN_PUMP
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·April 25, 2014
UNKNOWN_PUMP
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·April 25, 2014
UNKNOWN_PUMP
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·April 25, 2014