Airinspace B.V.
Country not established
- Devices
- 1
What Airinspace B.V. makes
Airinspace B.V. makes air purification devices, specifically the PLASMAIR model T2006, which is designed to reduce airborne contaminants using plasma-based technology.
The PLASMAIR, model T2006 is classified as a Class II medical device and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Plasmair, Model T2006 Ref K070722
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Airinspace B.V. have in the registry?
The registry currently lists 1 device for Airinspace B.V.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Airinspace B.V.'s devices?
Among its 1 most recently registered device, Airinspace B.V. has devices listed in FDA 510(k) (1 device).
What risk classes do Airinspace B.V.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Airinspace B.V.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Airinspace B.V. in the registry?
The most recently registered devices listed for Airinspace B.V. include PLASMAIR, MODEL T2006.