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Azure Biosystems Inc.

US

Last updated May 31, 2026

What Azure Biosystems Inc. makes

Azure Biosystems Inc. manufactures semi-automated thermal cycler nucleic acid amplification analysers designed for in vitro diagnostic (IVD) use in laboratory settings. These devices are intended for nucleic acid testing, including amplification and analysis of genetic material for diagnostic purposes.

The company’s products are classified as Class II medical devices under regulatory frameworks and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States.

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

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
032828687

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
Azure Cielo Dx Azure Cielo 3 Dx
FDA UDI
Class IIActive
Azure Cielo Dx Azure Cielo 6 Dx
FDA UDI
Class IIActive

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