1,453 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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ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM
FDA Adverse Event
Injury
·CODMAN AND SHURTLEFF, INC·Product code NJE·August 4, 2015
ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM
FDA Adverse Event
Injury
·CODMAN AND SHURTLEFF, INC·Product code NJE·August 4, 2015
ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM
FDA Adverse Event
Injury
·CODMAN AND SHURTLEFF, INC·Product code NJE·August 4, 2015
ONYX
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·August 31, 2023
Hammer, Reflex, Powered
FDA classification
FDA Class 2
·Hammer, Reflex, Powered
IKON OPTICS
FDA registration
IKON OPTICS·1 product·🇺🇸 United States
Eko Health, Inc.
FDA registration
Eko Health, Inc.·5 products·🇺🇸 United States
BIKO
FDA UDI
ORMESA SRL·08055715708996·Medical device intended for children/teens/adul...
BIKO
FDA UDI
ORMESA SRL·08055715709313·Medical device intended for children/teens/adul...
BIKO
FDA UDI
ORMESA SRL·08055715708828·Medical device intended for children/teens/adul...
BIKO
FDA UDI
ORMESA SRL·08055715708743·Medical device intended for children/teens/adul...
BIKO
FDA UDI
ORMESA SRL·08055715709108·Medical device intended for children/teens/adul...
BIKO
FDA UDI
ORMESA SRL·08055715709009·Medical device intended for children/teens/adul...
BIKO
FDA UDI
ORMESA SRL·08055715708903·Medical device intended for children/teens/adul...
BIKO
FDA UDI
ORMESA SRL·08055715709252·Medical device intended for children/teens/adul...
BIKO
FDA UDI
ORMESA SRL·08055715708910·Medical device intended for children/teens/adul...
BIKO
FDA UDI
ORMESA SRL·08055715708811·Medical device intended for children/teens/adul...
BIKO
FDA UDI
ORMESA SRL·08055715708859·Medical device intended for children/teens/adul...
BIKO
FDA UDI
ORMESA SRL·08055715708590·Medical device intended for children/teens/adul...
BIKO
FDA UDI
ORMESA SRL·08055715708712·Medical device intended for children/teens/adul...