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.
No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | WANDERCRAFT (FR) · FDA 3015000676 |
| Devices in EUDAMED | 8 |
| Country of registration | France |