EOVE SA
FR-MF-000002877 · France · PAU
EOVE SA is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 9 |
|---|
Among these devices, 9 are declared active, 5 with a measuring function.
Devices declared under this manufacturer
- AC-150 Ventilator
- AC-70 Secretion Management Device
- EO BAT9 Battery Pack
- EO-150 VENTILATOR
- EO-300 IPPB Device
- EO-70 Secretion Management Device
- MV-150 Ventilator
- MV-70 Secretion Management Device
- VEMO 150
Catalogue references include AC-150VNT, AC-70SMD, EO-150 VNT, EO-300VNT, EO-BATPCK, MV-150VNT.
European nomenclature codes declared: Z12030103, Z12159009, Z1203019080, Z12030103,Z12159009.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| 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 | 9 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | EOVE |
What it holds in Canada
| Licences on record | 3 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 2 |
| Class 3 devices | 1 |
| First licensed | 2016-10-27 |
Licence types: Single Device (3).
Licensed under: EO-150 VENTILATOR, EO-BAT9 PACK BATTERY, EO-70 SECRETION MANAGEMENT DEVICE.
North American profile: Canada only. EOVE SA holds a Canadian licence but was not found in the U.S. register.