Medviso AB
SE-MF-000003217 · Sweden · Lund
Medviso AB is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 5 |
|---|
Among these devices, 5 are declared active, 5 with a measuring function.
Devices declared under this manufacturer
- Segment 3DPrint
- Segment CMR
- Segment CT
Catalogue references include 07350010100027, 07350010100034, 07350010100041.
European nomenclature codes declared: Z129092.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | MEDVISO AB (SE) · FDA 3008962159 |
| Devices in EUDAMED | 5 |
| Country of registration | Sweden |
Device-level evidence
| Devices with a numeric GTIN | 5 |
|---|---|
| Found in the U.S. device database | 4 |
| Share | 80.0 % |
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: United States only. Medviso AB is registered in the United States but was not found in the Canadian register.