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Vitatron Medical BV

Country not established

Devices
19

What Vitatron Medical BV makes

Vitatron Medical BV manufactures cardiac pacemakers, including permanent and temporary electrode-based models, as well as external test pulse generators for pacing system testing. Their portfolio includes specific series such as the P4000, P1000, C4000, C1000, Series 2000, Series 3000, Vitalith S 3000, and S6001, alongside endocardial electrodes for direct heart stimulation.

The company’s devices are classified under FDA Class II and Class III, with regulatory submissions recorded in the FDA’s 510(k) clearance database. Their products are listed in the United States, where they comply with U.S. medical device regulations.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Vitatron Medical BV have in the registry?

The registry currently lists 19 devices for Vitatron Medical BV. Devices recorded under merged duplicate company entries are counted once.

Which registries list Vitatron Medical BV's devices?

Among its 19 most recently registered devices, Vitatron Medical BV has devices listed in FDA 510(k) (19 devices).

What risk classes do Vitatron Medical BV's devices fall under?

Among its 19 most recently registered devices, the classes recorded for Vitatron Medical BV's devices are Class II and Class III. Each device page shows its own class and authorisation.

What are the newest devices from Vitatron Medical BV in the registry?

The most recently registered devices listed for Vitatron Medical BV include PACEMAKERS, VITATRON'S, CARDIAC PACEMAKER P4000 SER. & P1000, CARDIAC PACEMAKER C4000, C1000 SER. and EXTERNAL TEST PULSE GENERATOR.

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