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Zhejiang Lude Technology Development Co., Ltd.

ChinaFDA 510(k) applicant, unverified

Devices
1

What Zhejiang Lude Technology Development Co., Ltd. makes

The company manufactures aneroid sphygmomanometers, including models like the QL-50, QL-20, and QL-201, which are blood pressure measurement devices paired with stethoscopes for auscultatory readings.

These devices fall under FDA Class II regulation and are listed 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

Frequently asked questions

How many devices does Zhejiang Lude Technology Development Co., Ltd. have in the registry?

The registry currently lists 1 device for Zhejiang Lude Technology Development Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Zhejiang Lude Technology Development Co., Ltd.'s devices?

Among its 1 most recently registered device, Zhejiang Lude Technology Development Co., Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Zhejiang Lude Technology Development Co., Ltd.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Zhejiang Lude Technology Development Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Zhejiang Lude Technology Development Co., Ltd. in the registry?

The most recently registered devices listed for Zhejiang Lude Technology Development Co., Ltd. include Aneroid sphygmomanometer with stethoscope, QL-50, Aneroid sphygmomanometer, QL-20, Aneroid sphygmomanometer, QL-201.

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