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Cardiopulmonary Corp.

United StatesFDA applicant, unverified

Devices
9

What Cardiopulmonary Corp. makes

Cardiopulmonary Corp. manufactures and modifies ventilator systems, including the Venturi Ventilator and Bernoulli Ventilator, alongside associated management software solutions. Their portfolio includes standalone ventilator devices and software platforms like the Bernoulli Management System, Bernoulli Enterprise Software, and OXINET III integration. Updates and modifications to ventilator management software are also part of their offerings.

The company’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. Their products are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue9

Newest first, rows 1-9 of 9

Frequently asked questions

How many devices does Cardiopulmonary Corp. have in the registry?

The registry currently lists 9 devices for Cardiopulmonary Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Cardiopulmonary Corp.'s devices?

Among its 9 most recently registered devices, Cardiopulmonary Corp. has devices listed in FDA 510(k) (9 devices).

What risk classes do Cardiopulmonary Corp.'s devices fall under?

Among its 9 most recently registered devices, the classes recorded for Cardiopulmonary Corp.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Cardiopulmonary Corp. in the registry?

The most recently registered devices listed for Cardiopulmonary Corp. include MODIFICATION TO BERNOULLI VENTILATOR MANAGEMENT SYSTEM SOFTWARE, VENTURI VENTILATOR, MODIFICATION OF VENTURI VENTILATOR and BERNOULLI MANAGEMENT SYSTEM (MS) SOFTWARE.

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