Deep Breeze, Ltd.
Country not established
- Devices
- 3
What Deep Breeze, Ltd. makes
Deep Breeze, Ltd. manufactures a range of medical devices including the VRLXP Model XP, a VR lung electrosonograph, and the VRIICU system, each designed for clinical use in respiratory and intensive care settings.
All of these devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Vrlxp, Model Xp Ref K091732
Regimes: 510(k) Registry: 510(k)Vr Lung Electrosonograph Ref K061495
Regimes: 510(k) Registry: 510(k)Vriicu System Ref K073582
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Deep Breeze, Ltd. have in the registry?
The registry currently lists 3 devices for Deep Breeze, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Deep Breeze, Ltd.'s devices?
Among its 3 most recently registered devices, Deep Breeze, Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Deep Breeze, Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Deep Breeze, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Deep Breeze, Ltd. in the registry?
The most recently registered devices listed for Deep Breeze, Ltd. include VRLXP, MODEL XP, VR LUNG ELECTROSONOGRAPH and VRIICU SYSTEM.