Inverdia AB
SE-MF-000047520 · Sweden · Bromma
Inverdia AB is registered in the European database on medical devices as a manufacturer, with 95 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 95 |
|---|
Devices declared under this manufacturer
- Venoline 140 den
- Venoline FAS
- Venoline On
Showing 12 of 95 declared devices.
Catalogue references include VN433XSNU, VN434SBL, VN434XLBL, VN434XLSA, VN700GMS, VN701DXL.
European nomenclature codes declared: M030405, A13.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 95 |
| 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 | 95 |
|---|---|
| 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. Inverdia AB was not found in either the U.S. or the Canadian register.