# Azmed

> Medical device manufacturer record on deviCERTS, compiled from public registries. Azmed is a medical device manufacturer based in France, with 9 devices listed in EUDAMED, FDA 510(k) and FDA GUDID (FDA Class II; EU Class IIa) as of 15 Nov 2026.

- Canonical page: <https://devicerts.com/manufacturers/azmed>
- Country: France (from SRN)
- EUDAMED actor status: active
- Role: Manufacturer
- Registrations: EUDAMED, FDA
- EUDAMED SRN: FR-MF-000014277
- FDA FEI: 3026753394
- DUNS: 271425256

## Figures

- Devices: 9
- EU certificates: 1
- FDA recalls (matched to the firm by name): 0
- FDA establishments: 1

## Registry facts

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

- Registries: EUDAMED 3, FDA 510(k) 3, FDA GUDID 3
- Device classes: FDA Class II 6, EU Class IIa 3
- EMDN [Z11 Bioimaging and radiotherapy instruments](https://devicerts.com/categories/emdn/Z11): 3 devices

## Devices

The first 9 of 9, in the order of the canonical page, which lists them all.

- [Rayvolve 7](https://devicerts.com/devices/rayvolve-7-394009b8) · Class II · GUDID · status: Active
- [Rayvolve 7](https://devicerts.com/devices/rayvolve-7-ef5a557e) · Class II · GUDID · status: Active
- [Rayvolve 7](https://devicerts.com/devices/rayvolve-7) · Class II · GUDID · status: Active
- [Rayvolve](https://devicerts.com/devices/rayvolve-rayvolve-vm-cloud-ve-37700180) · ref Rayvolve - VM + Cloud (version 8) · Class IIa · EUDAMED · status: Active
- [Rayvolve AZchest](https://devicerts.com/devices/rayvolve-azchest-qbs) · ref K261378 · Class II · 510(k) · status: Active · decision 2026-08-28
- [Rayvolve](https://devicerts.com/devices/rayvolve-rayvolve-on-premise-f4b6b667) · ref Rayvolve - On-premise (Version 5) · Class IIa · EUDAMED · status: Active
- [Rayvolve PTX-PE](https://devicerts.com/devices/rayvolve-ptx-pe-qfm) · ref K243808 · Class II · 510(k) · status: Active · decision 2025-03-21
- [Rayvolve LN](https://devicerts.com/devices/rayvolve-ln-myn) · ref K243831 · Class II · 510(k) · status: Active · decision 2025-03-26
- [Rayvolve](https://devicerts.com/devices/rayvolve-rayvolve-on-premise) · ref Rayvolve- On premise (Version 2) · Class IIa · EUDAMED · status: Active

## EU certificates

- MDR 731678 · Quality management system · MDR · notified body BSI Group The Netherlands B.V. · issued 2026-04-08 · expires 2031-04-13 · status: reissued

## Source and citation

- Cite as: Azmed. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/azmed (data as of 2026-11-15).
- Data sources: [EUDAMED](https://ec.europa.eu/tools/eudamed), [FDA 510(k)](https://open.fda.gov/apis/device/510k/), [FDA GUDID](https://accessgudid.nlm.nih.gov/), [FDA registration and listing](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfrl/rl.cfm)
- 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/azmed.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/azmed
- 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.