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Rusch Intl.

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Devices
43

What Rusch Intl. makes

Rusch Intl. manufactures medical devices for airway management, including endotracheal tubes (plain Magill/Murphy and microlaryngeal styles), tracheostomy sets (TracheoFix-Set), and cuff pressure monitors (EndoTest). Their portfolio also covers urinary catheterization solutions such as intermittent urethral catheters, self-cath sets, and safety catheters, as well as epidural catheter models for pain management. Lubricating gels (Floneil, Flocath Introgel) and nasal/oral airway tubes (Rusch Miller-Abbott tube) are also part of their offerings.

These devices are classified under FDA categories Class I, Class II, and Unclassified (U), with regulatory submissions recorded in the FDA’s 510(k) clearance database. The company’s products are listed under U.S. jurisdiction, adhering to FDA requirements for medical device authorisation.

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

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Frequently asked questions

How many devices does Rusch Intl. have in the registry?

The registry currently lists 43 devices for Rusch Intl.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Rusch Intl.'s devices?

Among its 43 most recently registered devices, Rusch Intl. has devices listed in FDA 510(k) (43 devices).

What risk classes do Rusch Intl.'s devices fall under?

Among its 43 most recently registered devices, the classes recorded for Rusch Intl.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Rusch Intl. in the registry?

The most recently registered devices listed for Rusch Intl. include EPIDURAL CATHETER MODELS 1210/1200, FLOCATH, INTERMITTENT URETHRAL CATHETERS and RUSCH MILLER-ABBOTT TUBE.

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