Advance Medical Integration Systems
FR-MF-000014717 · France · Trégueux
Advance Medical Integration Systems is registered in the European database on medical devices as a manufacturer, with 44 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 44 |
|---|
Most frequent device types declared: ENDOBOTLE, ENDOBOTTLE, ENDOKIT, ENDOPUMP.
Among these devices, 10 are declared sterile.
Devices declared under this manufacturer
- 50100
- 50110
- 50290
- 60160
- 60260
- 60270
- 60450
- 60470
- 70100
- 80330
- 80600
- 85520
Showing 12 of 44 declared devices.
Catalogue references include 50100, 50110, 50290, 60160, 70100, 80330.
European nomenclature codes declared: G0380.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 44 |
| 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 | 44 |
|---|---|
| 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. Advance Medical Integration Systems was not found in either the U.S. or the Canadian register.