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Eumed Biotechnology Co., Ltd.

TaiwanFDA 510(k) applicant, unverified

Devices
2

What Eumed Biotechnology Co., Ltd. makes

Eumed Biotechnology Co., Ltd. manufactures the EUKARE, a medical device designed for [specific application not detailed], and the EUSURE Blood Glucose Monitoring System, a device for continuous or intermittent blood glucose level assessment in diabetic patients.

The company’s portfolio is regulated under Class II devices in the US and includes products listed via FDA 510(k) clearance. The manufacturer is based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Eukare Ref K062892

    Class II
    Active 510(k) 510(k) II
  • Eusure Blood Glucose Monitoring System Ref K040678

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does Eumed Biotechnology Co., Ltd. have in the registry?

The registry currently lists 2 devices for Eumed Biotechnology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Eumed Biotechnology Co., Ltd.'s devices?

Among its 2 most recently registered devices, Eumed Biotechnology Co., Ltd. has devices listed in FDA 510(k) (2 devices).

What risk classes do Eumed Biotechnology Co., Ltd.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Eumed Biotechnology Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Eumed Biotechnology Co., Ltd. in the registry?

The most recently registered devices listed for Eumed Biotechnology Co., Ltd. include EUKARE and EUSURE BLOOD GLUCOSE MONITORING SYSTEM.

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