# Fizimed

> Medical device manufacturer record on deviCERTS, compiled from public registries. Fizimed is a medical device manufacturer based in France, with 3 devices listed in EUDAMED and FDA GUDID (EU Class I; FDA Class II) as of 15 Nov 2026.

- Canonical page: <https://devicerts.com/manufacturers/fizimed>
- Country: France (from SRN)
- EUDAMED actor status: active
- Role: Manufacturer
- Registrations: EUDAMED
- EUDAMED SRN: FR-MF-000011804
- DUNS: 269584479

## Figures

- Devices: 3
- FDA recalls (matched to the firm by name): 0

## Registry facts

*Every device of the manufacturer. A device listed in two registries counts in both.*

- Registries: EUDAMED 2, FDA GUDID 1
- Device classes: EU Class I 2, FDA Class II 1
- EMDN [U07 Devices for the treatment of incontinence](https://devicerts.com/categories/emdn/U07): 2 devices

## Devices

The first 3 of 3, in the order of the canonical page, which lists them all.

- [Fizimed Emy V1](https://devicerts.com/devices/fizimed-emy-v1) · Class II · GUDID · status: Listed
- [Emy application](https://devicerts.com/devices/emy-application-app-v9) · ref APP V9 · Class I · EUDAMED · status: Active
- [Emy Trainer](https://devicerts.com/devices/emy-trainer-emy-eg) · ref Emy EG · Class I · EUDAMED · status: Withdrawn

## Source and citation

- Cite as: Fizimed. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/fizimed (data as of 2026-11-15).
- Data sources: [EUDAMED](https://ec.europa.eu/tools/eudamed), [FDA GUDID](https://accessgudid.nlm.nih.gov/)
- EUDAMED record synced: 2026-11-07
- FDA recall data as of: 2026-11-01
- Data as of: 2026-11-15
- JSON: <https://devicerts.com/manufacturers/fizimed.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/manufacturers/fizimed
- 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.