Lumina Adhesives AB
SE-MF-000000737 · Sweden · GÖTEBORG
Lumina Adhesives AB is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 11 |
|---|
Among these devices, 11 are declared sterile.
Devices declared under this manufacturer
- Lumina Film dressing 10x12
- Lumina Film dressing 15x15
- Lumina Film dressing 5x7,2
- Lumina IV dressing 7x8,5
- Lumina IV dressing 8,5x11,5
- Lumina Post-op dressing 10x15
- Lumina Post-op dressing 10x25
- Lumina Post-op dressing 6x10
Catalogue references include 1000139, 1000141, 1000409, 1000410, 1000411, 1000412.
European nomenclature codes declared: M04040601, M04010102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 11 |
| 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 | 11 |
|---|---|
| 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. Lumina Adhesives AB was not found in either the U.S. or the Canadian register.