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Rabintex Industries, Ltd.

IsraelFDA applicant, unverified

Devices
1

What Rabintex Industries, Ltd. makes

Rabintex Industries, Ltd. manufactures the PERSHIELD CPR Device, a mechanical aid designed to assist in cardiopulmonary resuscitation by providing chest compressions during resuscitation efforts.

The PERSHIELD CPR Device 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

  • Pershield Cpr Device Ref K940820

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

Frequently asked questions

How many devices does Rabintex Industries, Ltd. have in the registry?

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

Which registries list Rabintex Industries, Ltd.'s devices?

Among its 1 most recently registered device, Rabintex Industries, Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Rabintex Industries, Ltd.'s devices fall under?

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

What are the newest devices from Rabintex Industries, Ltd. in the registry?

The most recently registered devices listed for Rabintex Industries, Ltd. include PERSHIELD CPR DEVICE.

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