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Diagnosis Related Systems, Inc.

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Devices
1

What Diagnosis Related Systems, Inc. makes

Diagnosis Related Systems, Inc. manufactures the BIODOP™, a diagnostic device designed for blood doping analysis, which detects erythropoietin (EPO) and other performance-enhancing substances in blood samples.

The BIODOP™ is classified as a Class II medical device under FDA regulations and is authorised via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Biodop(Tm) Ref K883334

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Diagnosis Related Systems, Inc. have in the registry?

The registry currently lists 1 device for Diagnosis Related Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Diagnosis Related Systems, Inc.'s devices?

Among its 1 most recently registered device, Diagnosis Related Systems, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Diagnosis Related Systems, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Diagnosis Related Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Diagnosis Related Systems, Inc. in the registry?

The most recently registered devices listed for Diagnosis Related Systems, Inc. include BIODOP(TM).

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