Medivent Limited
United KingdomFDA applicant, unverified
- Devices
- 1
What Medivent Limited makes
Medivent Limited manufactures the RTX Respirator, a medical device designed for mechanical ventilation support in clinical settings. This device is intended for patients requiring assisted or controlled breathing, including those in intensive care or during surgical procedures.
The RTX Respirator is classified as a Class II device under regulatory frameworks and has been authorised through the FDA’s 510(k) clearance process. The company is based in the United States.
Catalogue
Rtx Respirator Ref K082657
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medivent Limited have in the registry?
The registry currently lists 1 device for Medivent Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medivent Limited's devices?
Among its 1 most recently registered device, Medivent Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Medivent Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medivent Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medivent Limited in the registry?
The most recently registered devices listed for Medivent Limited include RTX RESPIRATOR.