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Rapid City Regional Hospital, Inc.

United StatesFDA applicant, unverified

Devices
10

What Rapid City Regional Hospital, Inc. makes

The manufacturer produces microbiological culture media and transport media, including nonselective and nondifferential agar plates (e.g., Mueller Hinton, Sabouraud’s Dextrose), selective and differential agars (e.g., Eosin Methylene Blue, XLD), broths (e.g., Selenite F, Bile E), and specialized diagnostic media (e.g., Christensen’s Urea Agar, DNase Test Media). These products support bacterial, fungal, and biochemical identification in clinical and research settings.

The portfolio includes Class I and Class II devices, with submissions recorded in the FDA’s 510(k) registry. The company is based in the United States.

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

Catalogue10

Newest first, rows 1-10 of 10

Frequently asked questions

How many devices does Rapid City Regional Hospital, Inc. have in the registry?

The registry currently lists 10 devices for Rapid City Regional Hospital, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Rapid City Regional Hospital, Inc.'s devices?

Among its 10 most recently registered devices, Rapid City Regional Hospital, Inc. has devices listed in FDA 510(k) (10 devices).

What risk classes do Rapid City Regional Hospital, Inc.'s devices fall under?

Among its 10 most recently registered devices, the classes recorded for Rapid City Regional Hospital, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Rapid City Regional Hospital, Inc. in the registry?

The most recently registered devices listed for Rapid City Regional Hospital, Inc. include CULTURE MEDIA NONSELECTIVE & NONDIFFERENTIAL, MUELLER HINTON AGAR, MARTIN LEWIS AGAR and CORN MEAL AGAR.

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