Alertis Medical AS
Country not established
- Devices
- 1
What Alertis Medical AS makes
Alertis Medical AS manufactures the ISCALERT Sensor System, a device designed for continuous, non-invasive monitoring of intracranial pressure (ICP) in clinical settings. This system is intended to provide real-time data to support patient management in critical care environments, particularly for conditions requiring ICP monitoring.
The ISCALERT Sensor System is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Iscalert Sensor System Ref K071165
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alertis Medical AS have in the registry?
The registry currently lists 1 device for Alertis Medical AS. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alertis Medical AS's devices?
Among its 1 most recently registered device, Alertis Medical AS has devices listed in FDA 510(k) (1 device).
What risk classes do Alertis Medical AS's devices fall under?
Among its 1 most recently registered device, the classes recorded for Alertis Medical AS's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alertis Medical AS in the registry?
The most recently registered devices listed for Alertis Medical AS include ISCALERT SENSOR SYSTEM.