Wandercraft
FR-MF-000000814 · France · Paris
Wandercraft is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 8 |
|---|
Most frequent device types declared: ATA-002-FR, V5-019-FR.
Among these devices, 8 are declared active.
Devices declared under this manufacturer
- Atalante
- Atalante X
- Atalante X [EN]
- Atalante X [ES]
- Atalante [ES]
- Atalante [FR]
Catalogue references include ATA-002-DE, ATA-002-EN, ATA-002-ES, ATA-002-FR, ATA-002-IT, V5-019-FR.
European nomenclature codes declared: Y061218.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | WANDERCRAFT (FR) · FDA 3015000676 |
| Devices in EUDAMED | 8 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 8 |
|---|---|
| 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: United States only. Wandercraft is registered in the United States but was not found in the Canadian register.