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Uniphy Elektromedizin GmbH & Co. KG

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Devices
1

What Uniphy Elektromedizin GmbH & Co. KG makes

Uniphy Elektromedizin GmbH & Co. KG manufactures cryotherapy devices, specifically the CRYOFLOW 700 and CRYOFLOW 1000 models.

These devices are listed in the FDA 510(k) registry and are classified as Class II medical devices. The company is based in the US.

AI-generated from registry data, 28 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Cryoflow 700, Cryoflow 1000 Ref K052310

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

Frequently asked questions

How many devices does Uniphy Elektromedizin GmbH & Co. KG have in the registry?

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

Which registries list Uniphy Elektromedizin GmbH & Co. KG's devices?

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

What risk classes do Uniphy Elektromedizin GmbH & Co. KG's devices fall under?

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

What are the newest devices from Uniphy Elektromedizin GmbH & Co. KG in the registry?

The most recently registered devices listed for Uniphy Elektromedizin GmbH & Co. KG include CRYOFLOW 700, CRYOFLOW 1000.

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