Trident Industri AB
SE-MF-000044390 · Sweden · Ängelholm
Trident Industri AB is registered in the European database on medical devices as a manufacturer, with 17 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 17 |
|---|
Most frequent device types declared: HomeAccess.
Devices declared under this manufacturer
- Rampmodul 0.9x0.5 A (2)
- Rampmodul 0.9x0.5 A (3)
- Rampmodul 0.9x1.0 A (3)
- Rampmodul 0.9x2.0 A (2)
- Rampmodul 0.9x2.0 A (3)
- Rampmodul 1.4x0.5 A (2)
- Rampmodul 1.4x0.5 A (3)
- Rampmodul 1.4x1.0 A (3)
- Rampmodul 1.4x2.0 A (2)
- Stolpe A DR 0.9
- Stolpe A P/K 0.9
- Stolpe A R 0.9
Showing 12 of 17 declared devices.
Catalogue references include 200707, 201033, 201061, 201082, 201156, 201431.
European nomenclature codes declared: Y181899.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 17 |
| Country of registration | Sweden |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 17 |
|---|---|
| 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. Trident Industri AB was not found in either the U.S. or the Canadian register.