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Vesper Medical, Inc.

United States·US-MF-000002025

Last updated June 8, 2026

Information

Country: United States
Address: 5905, Nathan Lane North, Plymouth, United States
Website: philips.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: —
PRRC Contact: Chad Wieneke
EUDAMED SRN: US-MF-000002025
FDA FEI Number: —
DUNS Number: 080441571

Catalogue (14)

Device	Model / Reference	Registries	Class	Status
Duo Hybrid Venous Stent System	N1101414009120	FDA UDI	Class III	Active
Duo Hybrid Venous Stent System	N1101614010120	FDA UDI	Class III	Active
Duo Extend Venous Stent System	N1201208009120	FDA UDI	Class III	Active
Duo Hybrid Venous Stent System	N1101616010120	FDA UDI	Class III	Active
Duo Hybrid Venous Stent System	N1101416009120	FDA UDI	Class III	Active
Duo Hybrid Venous Stent System	N1101412009120	FDA UDI	Class III	Active
Duo Hybrid Venous Stent System	N1101612010120	FDA UDI	Class III	Active
Duo Extend Venous Stent System	N1201212009120	FDA UDI	Class III	Active
Duo Hybrid Venous Stent System	N1101410009120	FDA UDI	Class III	Active
Duo Hybrid Venous Stent System	N1101812010120	FDA UDI	Class III	Active
Duo Hybrid Venous Stent System	N1101610010120	FDA UDI	Class III	Active
Duo Extend Venous Stent System	N1201412009120	FDA UDI	Class III	Active
Duo Extend Venous Stent System	N1201408009120	FDA UDI	Class III	Active
Duo Extend Venous Stent System	N1201612010120	FDA UDI	Class III	Active

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