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Stockert Instrumente GmbH

Country not established

Devices
9

What Stockert Instrumente GmbH makes

Stockert Instrumente GmbH manufactures cardiac perfusion devices, including coronary and venous cannulae, centrifugal pumps, and purge control systems for use during open-heart surgery. Their portfolio includes dedicated pediatric aortic cannulae, pump consoles, and alarm amplifiers designed for intraoperative blood circulation support.

These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company operates from the United States.

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

Catalogue9

Newest first, rows 1-9 of 9

Frequently asked questions

How many devices does Stockert Instrumente GmbH have in the registry?

The registry currently lists 9 devices for Stockert Instrumente GmbH. Devices recorded under merged duplicate company entries are counted once.

Which registries list Stockert Instrumente GmbH's devices?

Among its 9 most recently registered devices, Stockert Instrumente GmbH has devices listed in FDA 510(k) (9 devices).

What risk classes do Stockert Instrumente GmbH's devices fall under?

Among its 9 most recently registered devices, the classes recorded for Stockert Instrumente GmbH's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Stockert Instrumente GmbH in the registry?

The most recently registered devices listed for Stockert Instrumente GmbH include STOCKERT CORONARY PERFUSION CANNULAE, CENTRIFUGAL PUMP, STOCKERTIR PURGE CONTROL (APC) SYSTEM and STOCKERT CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP.

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