Topro Industri AS
NO-MF-000003447 · Norway · Gjøvik
Topro Industri AS is registered in the European database on medical devices as a manufacturer, with 87 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 87 |
|---|
Most frequent device types declared: TAURUS E, TAURUS H, TOPRO Olympos ATR, TOPRO TROJA ORGINAL.
Devices declared under this manufacturer
- Olympos ATR 'Black Series' M, Polarsilber, OFF road wheels
- Olympos ATR 'Black Series' S, Bordeauxrot, OFF road wheels
- Olympos ATR 'Black Series' S, Nachtschwarz, OFF road wheels
- TOPRO OLYMPOS ATR BS M (SI) SE
- TOPRO OLYMPOS ATR M (SI)
- TOPRO TAURUS H BASIC
- Troja 5G 'Black Series' M, Bordeauxrot
- Troja 5G 'Black Series' M, Ozeanblau
- Troja 5G 'Black Series' M, Polarsilber
- Troja 5G 'Black Series' S, Bordeauxrot
- Troja Original 'Black Series' M, Nachtschwarz
- Troja Original 'Black Series' M, Polarsilber
Showing 12 of 87 declared devices.
Catalogue references include 110501, 111500, 113501, 113511, 114561, 120000.
European nomenclature codes declared: Y120609, Y120606.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 87 |
| Country of registration | Norway |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 87 |
|---|---|
| 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. Topro Industri AS was not found in either the U.S. or the Canadian register.