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Razek Equipamentos Ltda

Country not established

Devices
11,827

What Razek Equipamentos Ltda makes

The company produces single-use orthopaedic burs designed for surgical procedures, as well as reusable orthopaedic surgical procedure kits that do not contain medications. These tools are intended for use in orthopaedic surgeries where precision cutting or preparation of bone is required.

The portfolio consists of Class I devices, which are generally considered to pose the lowest risk and are subject to minimal regulatory oversight. These devices are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. regulatory requirements. The manufacturer is based in the United States.

AI-generated from registry data, 19 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue11,827

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Company details

DUNS number
898213154

Sites1

Frequently asked questions

How many devices does RAZEK EQUIPAMENTOS LTDA have in the registry?

The registry currently lists 11827 devices for RAZEK EQUIPAMENTOS LTDA. Devices recorded under merged duplicate company entries are counted once.

Which registries list RAZEK EQUIPAMENTOS LTDA's devices?

Among its 50 most recently registered devices, RAZEK EQUIPAMENTOS LTDA has devices listed in FDA GUDID (50 devices).

What risk classes do RAZEK EQUIPAMENTOS LTDA's devices fall under?

Among its 50 most recently registered devices, the classes recorded for RAZEK EQUIPAMENTOS LTDA's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from RAZEK EQUIPAMENTOS LTDA in the registry?

The most recently registered devices listed for RAZEK EQUIPAMENTOS LTDA include RAZEK EQUIPAMENTOS 736990300, RAZEK EQUIPAMENTOS 730170006, RAZEK EQUIPAMENTOS 978840400 and RAZEK EQUIPAMENTOS 733622100.

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