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The Heart Valve Div. Medtronic Cardiovascular Surg

Country not established

Devices
5

What The Heart Valve Div. Medtronic Cardiovascular Surg makes

The company manufactures temporary myocardial pacing wires, including unipolar leads for adult and pediatric use, and flexible annuloplasty rings for heart valve repair, such as the Duran Flex models and posterior annuloplasty bands.

These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The manufacturer is based in the United States.

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

Catalogue5

Newest first, rows 1-5 of 5

Frequently asked questions

How many devices does The Heart Valve Div. Medtronic Cardiovascular Surg have in the registry?

The registry currently lists 5 devices for The Heart Valve Div. Medtronic Cardiovascular Surg. Devices recorded under merged duplicate company entries are counted once.

Which registries list The Heart Valve Div. Medtronic Cardiovascular Surg's devices?

Among its 5 most recently registered devices, The Heart Valve Div. Medtronic Cardiovascular Surg has devices listed in FDA 510(k) (5 devices).

What risk classes do The Heart Valve Div. Medtronic Cardiovascular Surg's devices fall under?

Among its 5 most recently registered devices, the classes recorded for The Heart Valve Div. Medtronic Cardiovascular Surg's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from The Heart Valve Div. Medtronic Cardiovascular Surg in the registry?

The most recently registered devices listed for The Heart Valve Div. Medtronic Cardiovascular Surg include UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE, 6493, DURAN FLEXIBLE ANNULOPLASTY RING MODEL NUMBER H608H, UNIPOLAR PEDIATRIC TEMPORARY PACING LEAD, MODEL 6491 and DURAN FLEX ANNULOPLASTY RING/OBTUR H601H, MODIFIED.

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