Skip to content

Bunnell Life Systems, Inc.

Country not established

Devices
1

What Bunnell Life Systems, Inc. makes

Bunnell Life Systems, Inc. manufactures the BLSI Ventilation Monitor, a device designed to monitor and display respiratory parameters in mechanical ventilation settings.

The company’s portfolio is regulated under FDA Class II devices and includes submissions via the 510(k) pathway. The manufacturer is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

Frequently asked questions

How many devices does Bunnell Life Systems, Inc. have in the registry?

The registry currently lists 1 device for Bunnell Life Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Bunnell Life Systems, Inc.'s devices?

Among its 1 most recently registered device, Bunnell Life Systems, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Bunnell Life Systems, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Bunnell Life Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Bunnell Life Systems, Inc. in the registry?

The most recently registered devices listed for Bunnell Life Systems, Inc. include BLSI VENTILATION MONITOR.

Generated automatically from registry data and not verified by a human reviewer.