Cnsystem Medizintechnik AG
AustriaFDA applicant, unverified
- Devices
- 1
What Cnsystem Medizintechnik AG makes
Cnsystem Medizintechnik AG manufactures non-invasive continuous blood pressure monitoring systems, including the CNAP Monitor 500I and 500AT. These devices provide real-time arterial pressure waveform analysis for clinical and intensive care settings, enabling continuous hemodynamic monitoring without invasive procedures.
The company’s portfolio is regulated under FDA Class II devices, with relevant products listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cnsystem Medizintechnik AG have in the registry?
The registry currently lists 1 device for Cnsystem Medizintechnik AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cnsystem Medizintechnik AG's devices?
Among its 1 most recently registered device, Cnsystem Medizintechnik AG has devices listed in FDA 510(k) (1 device).
What risk classes do Cnsystem Medizintechnik AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Cnsystem Medizintechnik AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cnsystem Medizintechnik AG in the registry?
The most recently registered devices listed for Cnsystem Medizintechnik AG include NON-INVASIVE CONTINUOUS BLOOD PRESSURE MONITORING SYSTEM CNAP MONITOR 500I, 500AT.