# EIDON UWF Module

> Active: European Union and United States. Medical device record on deviCERTS, compiled from public registries.

- Canonical page: <https://devicerts.com/devices/eidon-uwf-module-axwflme001>
- Manufacturer: [Centervue S.P.A.](https://devicerts.com/manufacturers/centervue-s-p-a) (Italy)
- Device class: Class I (EU MDR); Class II (US FDA)
- FDA product code: MYC
- EMDN: Z12120180 OPHTALMOLOGY ASSESSMENTS AND DIAGNOSIS INSTRUMENTS - HARDWARE ACCESSORIES
- GMDN: Ophthalmic fundus camera (10551)

## Registrations and authorizations

- **GUDID** · GUDID listing · United States · UDI-DI 08053677040123 · listed 2026-04-29 · status: Listed (GUDID: in commercial distribution)
- **EUDAMED** · CE/MDR · European Union · Basic UDI-DI 805367704EIDON-UWFDW · UDI-DI 08053677040123 · registered 2021-11-26 · status: Active
- **GUDID** · FDA 510(k) · United States · K211328 · decision 2021-08-19 · decision SESE · status: Active · from GUDID

## Recalls

No recall on record.

## Identity

- Trade name: EIDON [FDA GUDID (AccessGUDID)]
- Generic name: Ophthalmic fundus camera [FDA GUDID (AccessGUDID)]
- Model / Ref / Catalog: AXWFLME001 [EUDAMED, FDA GUDID (AccessGUDID)]; EIDON UWF Module [FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: 08053677040123 [EUDAMED, FDA GUDID (AccessGUDID)]
- Basic UDI-DI: 805367704EIDON-UWFDW [EUDAMED]
- Direct marketing DI: 08053677040123 [EUDAMED]
- 510(k) Number: K211328 [FDA GUDID (AccessGUDID)]
- FDA product code: MYC [FDA GUDID (AccessGUDID)]
- EMDN code: Z12120180 [EUDAMED]
- GMDN term: Ophthalmic fundus camera (10551) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class I [EUDAMED]; Class II [FDA GUDID (AccessGUDID)]
- Regulation number: 886.1570 [FDA GUDID (AccessGUDID)]
- EU registration type: Standard device [EUDAMED]
- EU market of registration: Italy [EUDAMED]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Properties

- Prescription use: Yes [FDA GUDID (AccessGUDID)]
- Lot / batch number: Yes [FDA GUDID (AccessGUDID)]
- Serial number: Yes [FDA GUDID (AccessGUDID)]
- Manufacturing date: Yes [FDA GUDID (AccessGUDID)]
- Supplied sterile: No [EUDAMED, FDA GUDID (AccessGUDID)]
- Sterilise before use: No [EUDAMED, FDA GUDID (AccessGUDID)]
- Single use: No [FDA GUDID (AccessGUDID)]
- Implantable: No [EUDAMED, FDA GUDID (AccessGUDID)]
- Reusable: No [EUDAMED]
- Contains latex: No [EUDAMED, FDA GUDID (AccessGUDID)]
- Reprocessed single-use device: No [EUDAMED]
- Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No [EUDAMED]
- Incorporates a substance derived from human blood or plasma: No [EUDAMED]
- Contains human tissues or cells: No [EUDAMED]
- Contains animal tissues or cells: No [EUDAMED]
- Contains endocrine-disrupting substances: No [EUDAMED]
- Administering medicine: No [EUDAMED]
- Measuring function: No [EUDAMED]
- Incorporates a medicinal substance: No [EUDAMED]
- Over-the-counter: No [FDA GUDID (AccessGUDID)]
- Convenience kit: No [FDA GUDID (AccessGUDID)]
- Combination product: No [FDA GUDID (AccessGUDID)]
- HCT/P: No [FDA GUDID (AccessGUDID)]
- Premarket exempt: No [FDA GUDID (AccessGUDID)]
- Expiration date: No [FDA GUDID (AccessGUDID)]

## Source and citation

- Cite as: EIDON UWF Module, Centervue S.P.A. deviCERTS medical device catalogue. https://devicerts.com/devices/eidon-uwf-module-axwflme001 (data as of 2026-11-15).
- Data sources: [EUDAMED](https://ec.europa.eu/tools/eudamed), [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/)
- Registry records last synced: 2026-10-23
- Statuses computed as of: 2026-11-15
- JSON: <https://devicerts.com/devices/eidon-uwf-module-axwflme001.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/devices/eidon-uwf-module-axwflme001
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.