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Hiltrode, Inc.(A/S) Subsidiary Munkenes A/S

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Devices
1

What Hiltrode, Inc.(A/S) Subsidiary Munkenes A/S makes

Hiltrode, Inc. (A/S) Subsidiary Munkenes A/S manufactures an ECG electrode system, a medical device used to acquire electrocardiogram signals from patients.

The ECG electrode system is classified as a Class II device and is listed in the FDA 510(k) registry. The company is based in the United States.

AI-generated from registry data, 24 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Ecg Electrode System Ref K873442

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

Frequently asked questions

How many devices does Hiltrode, Inc.(A/S) Subsidiary Munkenes A/S have in the registry?

The registry currently lists 1 device for Hiltrode, Inc.(A/S) Subsidiary Munkenes A/S. Devices recorded under merged duplicate company entries are counted once.

Which registries list Hiltrode, Inc.(A/S) Subsidiary Munkenes A/S's devices?

Among its 1 most recently registered device, Hiltrode, Inc.(A/S) Subsidiary Munkenes A/S has devices listed in FDA 510(k) (1 device).

What risk classes do Hiltrode, Inc.(A/S) Subsidiary Munkenes A/S's devices fall under?

Among its 1 most recently registered device, the classes recorded for Hiltrode, Inc.(A/S) Subsidiary Munkenes A/S's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Hiltrode, Inc.(A/S) Subsidiary Munkenes A/S in the registry?

The most recently registered devices listed for Hiltrode, Inc.(A/S) Subsidiary Munkenes A/S include ECG ELECTRODE SYSTEM.

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