Cambio Healthcare Systems AB
SE-MF-000001229 · Sweden · Linköping
Cambio Healthcare Systems AB is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 6 |
|---|
Among these devices, 6 are declared active.
Catalogue references include 2023.12, 3.12, Cambio CIS, Cambio COSMIC EHR 4.X, Cambio COSMIC EHR 5.X, Cambio MittVaccin Journal.
European nomenclature codes declared: V92.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| 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 | 5 |
|---|---|
| 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. Cambio Healthcare Systems AB was not found in either the U.S. or the Canadian register.