Critisense, Ltd.
Country not established
- Devices
- 2
What Critisense, Ltd. makes
Critisense, Ltd. manufactures the CRITIVIEW (Model CRV3), a medical device designed for continuous monitoring of critical physiological parameters, including blood pressure and other vital signs in clinical settings.
The company’s portfolio is regulated under Class II devices in the United States, with products listed via the FDA’s 510(k) clearance process. The devices are intended for use in the US market.
Catalogue
Critiview, Model CRV3 Ref K062977
510(k) 510(k)Critiview Ref K051145
510(k) 510(k)
Frequently asked questions
How many devices does Critisense, Ltd. have in the registry?
The registry currently lists 2 devices for Critisense, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Critisense, Ltd.'s devices?
Among its 2 most recently registered devices, Critisense, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Critisense, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Critisense, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Critisense, Ltd. in the registry?
The most recently registered devices listed for Critisense, Ltd. include CRITIVIEW, MODEL CRV3 and CRITIVIEW.