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Woodville Polymer Engineering, Ltd.

Country not established

Devices
1

What Woodville Polymer Engineering, Ltd. makes

Woodville Polymer Engineering, Ltd. manufactures the RHYS-DAVIES EXSANGUINATOR, a device designed for blood removal or drainage in medical procedures.

The RHYS-DAVIES EXSANGUINATOR is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. 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

  • Rhys-Davies Exsanguinator Ref K842963

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

Frequently asked questions

How many devices does Woodville Polymer Engineering, Ltd. have in the registry?

The registry currently lists 1 device for Woodville Polymer Engineering, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Woodville Polymer Engineering, Ltd.'s devices?

Among its 1 most recently registered device, Woodville Polymer Engineering, Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Woodville Polymer Engineering, Ltd.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Woodville Polymer Engineering, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Woodville Polymer Engineering, Ltd. in the registry?

The most recently registered devices listed for Woodville Polymer Engineering, Ltd. include RHYS-DAVIES EXSANGUINATOR.

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