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CENTERVUE SPA

US

Last updated May 30, 2026

Part of Centervue

What CENTERVUE SPA makes

CenterVue SpA manufactures scanning-laser retinal imaging systems, including the EIDON device, which captures detailed retinal scans for diagnostic evaluation.

The company’s portfolio is classified under FDA’s Class II regulatory category and is listed in the FDA’s Unique Device Identifier (UDI) database. 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.

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
338702316

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
Eidon RETIA
FDA UDI
Class IIActive

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