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Phs Medical GmbH

Country not established FDA

Devices
1
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

What Phs Medical GmbH makes

Phs Medical GmbH manufactures the C-PORT, a Class II injectable power port designed for intravenous access and medication delivery. This device is intended for repeated venous access in patients requiring long-term therapy, such as chemotherapy or total parenteral nutrition.

The C-PORT is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the U.S. regulatory database. The company 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

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Phs Medical GmbH Fuldabrueck Hesse · DE FEI 3004407880

Frequently asked questions

How many devices does Phs Medical GmbH have in the registry?

The registry currently lists 1 device for Phs Medical GmbH. Devices recorded under merged duplicate company entries are counted once.

Which registries list Phs Medical GmbH's devices?

Among its 1 most recently registered device, Phs Medical GmbH has devices listed in FDA 510(k) (1 device).

What risk classes do Phs Medical GmbH's devices fall under?

Among its 1 most recently registered device, the classes recorded for Phs Medical GmbH's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Phs Medical GmbH in the registry?

The most recently registered devices listed for Phs Medical GmbH include C-PORT - HP POWER INJECTABLE PORT.

Which FDA establishments are linked to Phs Medical GmbH?

1 FDA establishment is linked to Phs Medical GmbH in the registry; they are listed on the company page.

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