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MRI-Tech Sp. z o.o.

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Devices
1

What MRI-Tech Sp. z o.o. makes

Mri-Tech Sp. Zo.O. manufactures the CIRRUS OPEN, a medical imaging device designed for MRI compatibility, likely used in clinical or research settings for detailed soft tissue visualization.

The CIRRUS OPEN is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Cirrus Open Ref K090080

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

Frequently asked questions

How many devices does Mri-Tech Sp. Zo.O. have in the registry?

The registry currently lists 1 device for Mri-Tech Sp. Zo.O.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Mri-Tech Sp. Zo.O.'s devices?

Among its 1 most recently registered device, Mri-Tech Sp. Zo.O. has devices listed in FDA 510(k) (1 device).

What risk classes do Mri-Tech Sp. Zo.O.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Mri-Tech Sp. Zo.O.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Mri-Tech Sp. Zo.O. in the registry?

The most recently registered devices listed for Mri-Tech Sp. Zo.O. include CIRRUS OPEN.

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