Spiritus Technologies, LLC
Country not established
- Devices
- 1
What Spiritus Technologies, LLC makes
Spiritus Technologies, LLC manufactures the Spiritus Cuff Inflation Syringe, a device designed for controlled inflation and deflation of blood pressure cuffs, typically used in clinical and home monitoring settings.
The company’s product portfolio is regulated under FDA Class II devices and is listed via 510(k) premarket notifications. The manufacturer is based in the United States.
Catalogue
Spirtius Cuff Inflation Syringe Ref K112915
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spiritus Technologies, LLC have in the registry?
The registry currently lists 1 device for Spiritus Technologies, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spiritus Technologies, LLC's devices?
Among its 1 most recently registered device, Spiritus Technologies, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Spiritus Technologies, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Spiritus Technologies, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spiritus Technologies, LLC in the registry?
The most recently registered devices listed for Spiritus Technologies, LLC include SPIRTIUS CUFF INFLATION SYRINGE.