Clemondo AB
SE-MF-000041481 · Sweden · Helsingborg
Clemondo AB is registered in the European database on medical devices as a manufacturer, with 12 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 12 |
|---|
Devices declared under this manufacturer
- Liv Des +45
- Liv Des +72
- Liv Des +72 Wipes
- Liv Des 70
- Liv Des Special +50
Catalogue references include 1703M001, 17040005, 17049300, 1704M001, 17230001, 17230005.
European nomenclature codes declared: D99.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 12 |
| 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 | 12 |
|---|---|
| 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. Clemondo AB was not found in either the U.S. or the Canadian register.