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Central Media

Country not established

Devices
14

What Central Media makes

Central Media produces microbiological culture media for laboratory use, including selective, differential, and enrichment media for detecting and identifying bacteria such as coliforms, streptococci, and anaerobes. Their portfolio also covers specialized media for mycological (fungal) and Corynebacterium isolation, as well as ECG-based and carbohydrate fermentation media for diagnostic testing.

The company’s products are regulated under FDA’s 510(k) pathway, with devices classified as Class I and Class II. Their media are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Central Media have in the registry?

The registry currently lists 14 devices for Central Media. Devices recorded under merged duplicate company entries are counted once.

Which registries list Central Media's devices?

Among its 14 most recently registered devices, Central Media has devices listed in FDA 510(k) (14 devices).

What risk classes do Central Media's devices fall under?

Among its 14 most recently registered devices, the classes recorded for Central Media's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Central Media in the registry?

The most recently registered devices listed for Central Media include MUELLER HINTON MEDIA, MEDIA FOR DETECTION & VERIFICATION OF COLIFORMS, MIDDLEBROOK BASED MEDIA and ECG BASED MEDIA.

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