SURGIRIS
FR-MF-000004556 · France · CROIX
SURGIRIS is registered in the European database on medical devices as a manufacturer, with 155 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 155 |
|---|
Among these devices, 155 are declared active.
Devices declared under this manufacturer
- DERMARIS
- DIASYS
- EPURE
- EPURE 4
- EPURE 8
- X2MT
- X3MT
Showing 12 of 155 declared devices.
Catalogue references include ALIMMOB-020-NF-S0/A, ASS-ACC-041/B, ASS-ACC-046/B, ASS-ACC-064/B, EMERGILED-1S-4H/A, RM-ECL-S-03/F.
European nomenclature codes declared: Z12010780, Z12010701, Z12010702, Z11039010, Z12010785.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 155 |
| 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 | 155 |
|---|---|
| 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. SURGIRIS was not found in either the U.S. or the Canadian register.