Stasis Labs, Inc.
Country not established
- Devices
- 2
What Stasis Labs, Inc. makes
Stasis Labs, Inc. manufactures bedside monitoring systems designed to continuously track multiple physiological parameters in clinical settings. These devices are intended for real-time patient monitoring in environments such as hospitals and intensive care units, providing data on vital signs like heart rate, blood pressure, and oxygen saturation.
The company’s products fall under FDA Class II regulatory classification and are listed in the FDA’s 510(k) and UDI registries. The manufacturer is based in the United States.
Catalogue
- Registry: GUDID
Stasis Monitoring System Ref K183634
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 042605049
- [email protected]
- Phone
- 1.740.478.2747
Frequently asked questions
How many devices does Stasis Labs, Inc. have in the registry?
The registry currently lists 2 devices for Stasis Labs, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stasis Labs, Inc.'s devices?
Among its 2 most recently registered devices, Stasis Labs, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Stasis Labs, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Stasis Labs, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stasis Labs, Inc. in the registry?
The most recently registered devices listed for Stasis Labs, Inc. include Stasis Labs Stasis Monitoring System and Stasis Monitoring System.