Materialise Motion
BE-MF-000026574 · Belgium · Paal
Materialise Motion is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 5 |
|---|
Among these devices, 5 are declared active, 4 with a measuring function.
Devices declared under this manufacturer
- Footscan Pro Medium
- Footscan Pro Medium Sync
- Footscan Pro Small
- Footscan Pro Small Sync
- Materialise footscan software
Catalogue references include Footscan Pro Medium, Footscan Pro Medium Sync, Footscan Pro Small, Footscan Pro Small Sync, v26.1.
European nomenclature codes declared: Z12062603, Z12062692.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | Materialise Motion N.V. (BE) · FDA 3006543248 |
| Devices in EUDAMED | 5 |
| Country of registration | Belgium |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 5 |
|---|---|
| Found in the U.S. device database | 4 |
| Share | 80.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.