Medovent GmbH
GermanyFDA applicant, unverified
- Devices
- 2
What Medovent GmbH makes
Medovent GmbH manufactures the Reaxon Plus, a medical device designed for respiratory therapy, including non-invasive ventilation and continuous positive airway pressure (CPAP) applications.
The Reaxon Plus is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Reaxon Plus Ref K143711
Regimes: 510(k) Registry: 510(k)Reaxon Plus Ref K180222
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medovent GmbH have in the registry?
The registry currently lists 2 devices for Medovent GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medovent GmbH's devices?
Among its 2 most recently registered devices, Medovent GmbH has devices listed in FDA 510(k) (2 devices).
What risk classes do Medovent GmbH's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Medovent GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medovent GmbH in the registry?
The most recently registered devices listed for Medovent GmbH include Reaxon Plus.