exolis
FR-MF-000006271 · France · CESSON-SEVIGNE
exolis is registered in the European database on medical devices as a manufacturer, with 49 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 49 |
|---|
Most frequent device types declared: Exolis_Ref1, engageDM, exolis_ref1.
Devices declared under this manufacturer
- engage V7.1
- engage V7.12
- engage V7.13
- engage V7.14
- engage V7.19
- engage V7.2
- engage V7.21
- engage V7.26
- engage V7.3
- engage V7.31
- engage V7.33
- engage V7.4
Showing 12 of 49 declared devices.
Catalogue references include Exolis_Ref1, engageDM, exolis_Ref1, exolis_ref1.
European nomenclature codes declared: V92.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 49 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 49 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. exolis was not found in either the U.S. or the Canadian register.