5,256 results
·
38ms
·
Sources: EU EUDAMED, US FDA
QUO
FDA UDI
FGX INTERNATIONAL INC.·00193033442784·
QUO
FDA UDI
FGX INTERNATIONAL INC.·00193033207673·
QUO
FDA UDI
FGX INTERNATIONAL INC.·00057800230151·
QUO
FDA UDI
FGX INTERNATIONAL INC.·00193033428108·
QUO
FDA UDI
FGX INTERNATIONAL INC.·00193033464298·
QUO
FDA UDI
FGX INTERNATIONAL INC.·00193033368404·
QUO
FDA UDI
FGX INTERNATIONAL INC.·00193033507933·
QUO
FDA UDI
FGX INTERNATIONAL INC.·00057800096429·
EchoGo Heart Failure (2.0)
FDA 510(k)
FDA Class 2
·Cardiovascular
Vivio® LVEDP System
FDA 510(k)
FDA Class 2
·Cardiovascular
EchoGo Heart Failure
FDA 510(k)
FDA Class 2
·Cardiovascular
Adjunctive Heart Failure Status Indicator
FDA classification
FDA Class 2
·Adjunctive Heart Failure Status Indicator
Duo-Med
Manufacturer
🇧🇪 Belgium
Shih Kuo Enterprise Co., Ltd.
Manufacturer
🇹🇼 Taiwan
Aurix XL
FDA registration
NUO THERAPEUTICS, INC.·1 product·🇺🇸 United States
Aurix
FDA registration
NUO THERAPEUTICS, INC.·1 product·🇺🇸 United States
Aurix Multifly 4-Pack
FDA registration
NUO THERAPEUTICS, INC.·2 products·🇺🇸 United States
Clinic
FDA registration
LABORATORIOS CLINIC, S.A. DE C.V.·1 product·🇲🇽 Mexico
Changzhou Ou Nuo Medical Equipment Co., Ltd.
Manufacturer
🇨🇳 China·1 Basic UDI-DI·1 Device
MH2441A; MH2441A-E; MH2441A-J; MH2441A-P; MH2441A-R; MH2441A-W; MH2441AY; MH2441AZ;
FDA registration
AUO (SUZHOU) CO., LTD.·1 product·🇨🇳 China