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Mediserve Information Systems, Inc.

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Devices
1

What Mediserve Information Systems, Inc. makes

Mediserve Information Systems, Inc. manufactures the VentLink System, a medical device designed for ventilator management and patient monitoring in clinical settings.

The VentLink System is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company 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

  • Ventlink System Ref K052751

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Mediserve Information Systems, Inc. have in the registry?

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

Which registries list Mediserve Information Systems, Inc.'s devices?

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

What risk classes do Mediserve Information Systems, Inc.'s devices fall under?

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

What are the newest devices from Mediserve Information Systems, Inc. in the registry?

The most recently registered devices listed for Mediserve Information Systems, Inc. include VENTLINK SYSTEM.

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