Cellcomb
SE-MF-000008567 · Sweden · Säffle
Cellcomb is registered in the European database on medical devices as a manufacturer, with 71 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 71 |
|---|
Devices declared under this manufacturer
- Barrierelaken stort 160x310cm
- Biolam Lakan 150x270cm
- Biolam Plus Örngott 50x71cm
- Biolam Plus Örngott spärrskikt 35x40cm
- Cellbasic Underlägg 30x40cm (100-pack)
- Cellcombi Antihalk 100x240cm
- Cellcombi Slide Draglakan 78x140cm
- Cellcombi Slide Eco 100x240cm
- Cellcombi Slide Trauma/Op-lakan 100x240cm
- Cellcomfort Skyddslakan 80x210cm
- Cellcomfort Skyddslakan 80x90cm
- Cellstrong Extra Skyddslakan 80x250cm
Showing 12 of 71 declared devices.
Catalogue references include 100004, 106002, 394001, 394004, 397001, 702003.
European nomenclature codes declared: T030502, T04010299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 71 |
| 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 | 71 |
|---|---|
| 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. Cellcomb was not found in either the U.S. or the Canadian register.