Rayflow Italia S.r.l.
Country not established
- Devices
- 1
What Rayflow Italia S.r.l. makes
Rayflow Italia S.R.L. manufactures the Spiraflow 2001, a multi-directional tomographic imaging unit designed for detailed cross-sectional visualization of internal structures.
The company’s portfolio is regulated under the FDA’s 510(k) clearance process in the United States. The Spiraflow 2001 is listed as a Class II medical device, requiring pre-market notification to demonstrate substantial equivalence to a predicate device.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rayflow Italia S.R.L. have in the registry?
The registry currently lists 1 device for Rayflow Italia S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rayflow Italia S.R.L.'s devices?
Among its 1 most recently registered device, Rayflow Italia S.R.L. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Rayflow Italia S.R.L. in the registry?
The most recently registered devices listed for Rayflow Italia S.R.L. include SPIRAFLOW 2001, MULTI-DIRECTIONAL TOMOGRAPHIC UNIT.