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Medtronic Cardiac Surgical Products

Country not established

Devices
7

What Medtronic Cardiac Surgical Products makes

The company manufactures arterial and venous cannulae for cardiac surgical procedures, including models with pressure monitoring lines and 3D-tipped designs for improved vascular access. Products also include elongated single-piece arterial cannulae, malleable venous cannulae, and aortocoronary shunts with accompanying arteriotomy cannulae.

These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The portfolio is listed in the FDA’s 510(k) database, reflecting compliance with US medical device regulations.

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

Catalogue7

Newest first, rows 1-7 of 7

Frequently asked questions

How many devices does Medtronic Cardiac Surgical Products have in the registry?

The registry currently lists 7 devices for Medtronic Cardiac Surgical Products. Devices recorded under merged duplicate company entries are counted once.

Which registries list Medtronic Cardiac Surgical Products's devices?

Among its 7 most recently registered devices, Medtronic Cardiac Surgical Products has devices listed in FDA 510(k) (7 devices).

What risk classes do Medtronic Cardiac Surgical Products's devices fall under?

Among its 7 most recently registered devices, the classes recorded for Medtronic Cardiac Surgical Products's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Medtronic Cardiac Surgical Products in the registry?

The most recently registered devices listed for Medtronic Cardiac Surgical Products include MEDTRONIC DLP ARTERIAL CANNULA WITH 3D TIP - 22 FR., SELECT CAP ARTERIAL CANNULA WITH PRESSURE MONITORING LINE, MODEL 78818, 78820, 78822, 78824, 78918, 78920, 78922, 78924, 24 FR. LEFT HEART VENT CATHETER WITH PRESSURE MONITORING LINE, MODEL 12524 and MEDTRONIC DLP ARTERIAL CANNULAE WITH 3D TIP.

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