365 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Intracranial Aneurysm Flow Diverter
FDA Pre-Market Approval
FDA Class 3
·PIPELINE EMBOLIZATION DEVICE
Intracranial Aneurysm Flow Diverter
FDA Pre-Market Approval
FDA Class 3
·Pipeline Flex Embolization Device
Intracranial Aneurysm Flow Diverter
FDA Pre-Market Approval
FDA Class 3
·PIPELINE EMBOLIZATION DEVICE
Intracranial Aneurysm Flow Diverter
FDA Pre-Market Approval
FDA Class 3
·Pipeline Flex Embolization Device
Intracranial Aneurysm Flow Diverter
FDA Pre-Market Approval
FDA Class 3
·Pipeline Flex Embolization Device, Pipeline Flex Embolization Device with Shield Technology
Intracranial Aneurysm Flow Diverter
FDA Pre-Market Approval
FDA Class 3
·PIPELINE EMBOLIZATION DEVICE
Intracranial Aneurysm Flow Diverter
FDA Pre-Market Approval
FDA Class 3
·Pipeline Vantage Embolization Device with Shield Technology
Intracranial Aneurysm Flow Diverter
FDA Pre-Market Approval
FDA Class 3
·Pipeline Flex Embolization Device; Pipeline Flex Embolization Device with Shield Technology (Pipeline Shield)
Intracranial Aneurysm Flow Diverter
FDA Pre-Market Approval
FDA Class 3
·Pipeline Vantage Embolization Device with Shield Technology
Intracranial Aneurysm Flow Diverter
FDA Pre-Market Approval
FDA Class 3
·Pipeline Flex Embolization Device, Pipeline Flex Embolization Device with Shield Technology
Intracranial Aneurysm Flow Diverter
FDA Pre-Market Approval
FDA Class 3
·Pipeline Flex Embolization Device
Intracranial Aneurysm Flow Diverter
FDA Pre-Market Approval
FDA Class 3
·PIPELINE EMBOLIZATION DEVICE
Intracranial Aneurysm Flow Diverter
FDA Pre-Market Approval
FDA Class 3
·PIPELINE EMBOLIZATION DEVICE
Intracranial Aneurysm Flow Diverter
FDA Pre-Market Approval
FDA Class 3
·Pipeline Flex Embolization Device with Shield Technology (PED2), Pipeline Vantage Embolization Device with Shield Tec
Intracranial Aneurysm Flow Diverter
FDA Pre-Market Approval
FDA Class 3
·Pipeline Flex Embolization Device
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·LIFEPAK® 1000 Defibrillator
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·LIFEPAK® 35 Monitor/Defibrillator
Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm)
FDA Pre-Market Approval
FDA Class 3
·BIO-RAD MONOLISA ANTI-HBS EIA
Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm)
FDA Pre-Market Approval
FDA Class 3
·MONOLISA ANTI-HBC IGM EIA
Test, Hepatitis B (B Core, Be Antigen, Be Antibody, B Core Igm)
FDA Pre-Market Approval
FDA Class 3
·MONOLISA ANTI-HBS EIA