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Sign in to claim this brandWhat 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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- 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)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Eidon | RETIA | FDA UDI | Class II | Active |
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