Tayside Flow Technologies Limited
Country not established
- Devices
- 2
What Tayside Flow Technologies Limited makes
Tayside Flow Technologies Limited manufactures vascular grafts designed for arteriovenous access, including spiral laminar flow grafts and EPTFE-based spiral vascular grafts. These products are intended for surgical use in creating reliable vascular connections for hemodialysis patients.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II medical devices. These products are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Spiral Laminar Flow Vascular Arteriovenous Graft Ref K094044
Regimes: 510(k) Registry: 510(k)Eptfe Slftm Spiral Vascular Graft Ref K083169
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tayside Flow Technologies Limited have in the registry?
The registry currently lists 2 devices for Tayside Flow Technologies Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tayside Flow Technologies Limited's devices?
Among its 2 most recently registered devices, Tayside Flow Technologies Limited has devices listed in FDA 510(k) (2 devices).
What risk classes do Tayside Flow Technologies Limited's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Tayside Flow Technologies Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tayside Flow Technologies Limited in the registry?
The most recently registered devices listed for Tayside Flow Technologies Limited include SPIRAL LAMINAR FLOW VASCULAR ARTERIOVENOUS GRAFT and EPTFE SLFTM SPIRAL VASCULAR GRAFT.