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Caird Technology

Country not established

Devices
3

What Caird Technology makes

Caird Technology makes the Holter 2000, a spirometer, and the ANS System.

These devices are Class II medical devices listed in the FDA 510(k) registry, and the company is based in the United States.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • Caird Technology Holter 2000 Ref K012686

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Caird Technology Spirometer Ref K971336

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Ans System Ref K101016

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

Frequently asked questions

How many devices does Caird Technology have in the registry?

The registry currently lists 3 devices for Caird Technology. Devices recorded under merged duplicate company entries are counted once.

Which registries list Caird Technology's devices?

Among its 3 most recently registered devices, Caird Technology has devices listed in FDA 510(k) (3 devices).

What risk classes do Caird Technology's devices fall under?

Among its 3 most recently registered devices, the classes recorded for Caird Technology's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Caird Technology in the registry?

The most recently registered devices listed for Caird Technology include CAIRD TECHNOLOGY HOLTER 2000, CAIRD TECHNOLOGY SPIROMETER and ANS SYSTEM.

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