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A & Z Pharmaceutical Inc.

US

Last updated May 31, 2026

What A & Z Pharmaceutical Inc. makes

A & Z Pharmaceutical Inc. manufactures single-use, non-antimicrobial surgical and medical respirators designed for patient ventilation during medical procedures.

The company’s products are classified as Class II devices and are listed in the FDA’s Unique Device Identification (UDI) system. The manufacturer is based in the United States.

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 A & Z Pharmaceutical Inc. manufacture?

A & Z Pharmaceutical Inc. specializes in surgical and medical respirators that are designed for single-use and non-antimicrobial applications. These devices are intended for patient ventilation during medical procedures, ensuring temporary respiratory support in clinical settings.

Where is A & Z Pharmaceutical Inc. based?

A & Z Pharmaceutical Inc. is headquartered in the United States. The company’s location is relevant for regulatory compliance and distribution, as it operates within the U.S. healthcare system.

How are the devices manufactured by A & Z Pharmaceutical Inc. classified under regulatory standards?

The devices produced by A & Z Pharmaceutical Inc. fall under the classification of Class II medical devices. This classification typically applies to devices that pose moderate risk and require special controls to ensure safety and effectiveness, such as performance standards or post-market surveillance.

Are the devices from A & Z Pharmaceutical Inc. listed in any regulatory registries?

Yes, the devices manufactured by A & Z Pharmaceutical Inc. are included in the FDA’s Unique Device Identification (UDI) system. The UDI system helps track and trace medical devices throughout their distribution and use, improving patient safety and regulatory oversight.

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

Information

Country
US
Address
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LinkedIn
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Facebook
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Phone
800-480-1059
PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
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DUNS Number
926820705

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
A&Z Pharmaceutical M8004
FDA UDI
Class IIActive

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