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Mse Medizintechnik GmbH & Co. KG

GermanyFDA applicant, unverified

Devices
1

What Mse Medizintechnik GmbH & Co. KG makes

Mse Medizintechnik GmbH & Co. KG manufactures the POLYSCAN DIGITAL SCANNER, a device designed for digital imaging of polygraphic or other medical data.

The POLYSCAN DIGITAL SCANNER is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. 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

  • Polyscan Digital Scanner Ref K944684

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

Frequently asked questions

How many devices does Mse Medizintechnik GmbH & Co. KG have in the registry?

The registry currently lists 1 device for Mse Medizintechnik GmbH & Co. KG. Devices recorded under merged duplicate company entries are counted once.

Which registries list Mse Medizintechnik GmbH & Co. KG's devices?

Among its 1 most recently registered device, Mse Medizintechnik GmbH & Co. KG has devices listed in FDA 510(k) (1 device).

What risk classes do Mse Medizintechnik GmbH & Co. KG's devices fall under?

Among its 1 most recently registered device, the classes recorded for Mse Medizintechnik GmbH & Co. KG's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Mse Medizintechnik GmbH & Co. KG in the registry?

The most recently registered devices listed for Mse Medizintechnik GmbH & Co. KG include POLYSCAN DIGITAL SCANNER.

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