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P.T. Delta Waru Rubber Industry

ID Last updated 22 Oct 2026

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Devices
1
Registries
FDA 510(k)
FDA recalls
0

Catalogue1

What P.T. Delta Waru Rubber Industry makes

P.T. Delta Waru Rubber Industry manufactures latex examination gloves, designed for single-use medical and clinical applications to ensure barrier protection during procedures.

The company’s portfolio is regulated under FDA 510(k) clearance as Class I medical devices and is listed in the US regulatory registry.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does P.T. Delta Waru Rubber Industry manufacture?

P.T. Delta Waru Rubber Industry specializes in manufacturing latex examination gloves, which are intended for single-use medical and clinical applications. These gloves provide a barrier to protect both patients and healthcare workers during procedures, ensuring hygiene and safety.

Where is P.T. Delta Waru Rubber Industry based?

The company is based in the United States. Its operations are focused on producing medical-grade latex products regulated under US healthcare standards.

Which regulatory registries list P.T. Delta Waru Rubber Industry’s devices?

The company’s latex examination gloves are listed in the FDA 510(k) registry, as they are classified under Class I medical devices in the US regulatory framework. This classification applies to devices deemed to pose minimal risk.

How are P.T. Delta Waru Rubber Industry’s devices classified under US regulations?

The company’s latex examination gloves fall under Class I classification in the US. This classification is assigned to devices that present the lowest risk to patients and users, often requiring less stringent premarket review due to their well-established safety and performance.

AI-generated from registry data and not verified by a human reviewer.

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