Microlife Systems AG
Country not established
- Devices
- 1
What Microlife Systems AG makes
Microlife Systems AG manufactures blood pressure monitoring devices, including the MICROLIFE IT2CA1, which is designed for clinical and home use to measure and record blood pressure readings.
The company’s portfolio is regulated under Class II medical devices in the US, with devices listed via the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Microlife IT2CA1 Ref K990168
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Microlife Systems AG have in the registry?
The registry currently lists 1 device for Microlife Systems AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Microlife Systems AG's devices?
Among its 1 most recently registered device, Microlife Systems AG has devices listed in FDA 510(k) (1 device).
What risk classes do Microlife Systems AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Microlife Systems AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Microlife Systems AG in the registry?
The most recently registered devices listed for Microlife Systems AG include MICROLIFE IT2CA1.