Tereopneuma
Country not established
- Devices
- 1
What Tereopneuma makes
Tereopneuma manufactures the ReDe Mask, a respiratory device designed for non-invasive ventilation and continuous positive airway pressure (CPAP) therapy.
The ReDe Mask is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
ReDe Mask Ref K161953
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tereopneuma have in the registry?
The registry currently lists 1 device for Tereopneuma. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tereopneuma's devices?
Among its 1 most recently registered device, Tereopneuma has devices listed in FDA 510(k) (1 device).
What risk classes do Tereopneuma's devices fall under?
Among its 1 most recently registered device, the classes recorded for Tereopneuma's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tereopneuma in the registry?
The most recently registered devices listed for Tereopneuma include ReDe Mask.