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Canamet Canadian Natl Medical Technologies, Inc.

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Devices
1

What Canamet Canadian Natl Medical Technologies, Inc. makes

Canamet Canadian National Medical Technologies, Inc. manufactures the Piesometer, Model MK-1, a device designed for measuring pressure in medical applications, such as bladder or gastrointestinal monitoring.

The Piesometer, Model MK-1 is classified as a Class II medical device in the US and is listed under the FDA’s 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

  • Piesometer, Model Mk-1 Ref K041169

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

Frequently asked questions

How many devices does Canamet Canadian Natl Medical Technologies, Inc. have in the registry?

The registry currently lists 1 device for Canamet Canadian Natl Medical Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Canamet Canadian Natl Medical Technologies, Inc.'s devices?

Among its 1 most recently registered device, Canamet Canadian Natl Medical Technologies, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Canamet Canadian Natl Medical Technologies, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Canamet Canadian Natl Medical Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Canamet Canadian Natl Medical Technologies, Inc. in the registry?

The most recently registered devices listed for Canamet Canadian Natl Medical Technologies, Inc. include PIESOMETER, MODEL MK-1.

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