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E-Cath Co., Ltd.

Country not established

Devices
1

What E-Cath Co., Ltd. makes

E-Cath Co., Ltd. manufactures the PHTIP Disposable ISFET Catheter, a reusable or single-use medical device designed for intraprostatic temperature monitoring during therapeutic procedures.

The company’s portfolio is regulated under FDA’s Class II device classification and requires 510(k) clearance. The device is listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

Frequently asked questions

How many devices does E-Cath Co., Ltd. have in the registry?

The registry currently lists 1 device for E-Cath Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list E-Cath Co., Ltd.'s devices?

Among its 1 most recently registered device, E-Cath Co., Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do E-Cath Co., Ltd.'s devices fall under?

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

What are the newest devices from E-Cath Co., Ltd. in the registry?

The most recently registered devices listed for E-Cath Co., Ltd. include PHTIP DISPOSABLE ISFET CATHETER.

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