Oslo universitetssykehus HF
NO-MF-000028214 · Norway · Oslo
Oslo universitetssykehus HF is registered in the European database on medical devices as a manufacturer, with 73 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- Amøbe saltvann
- BCP agarskål
- CLAT agarskål
- Fastidious anaerob agarskål
- GC medium med isovitalex og hemoglobin
- Gentianafiolett fargeløsning 0,5%
- Legionella ikke-selektiv agarskål
- Legionella selektiv agarskål
- MH II agarskål med hemoglobin og isovitalex
- MH-F agarskål
- Safranin fargeløsning
- Selenitt medium
Showing 12 of 73 declared devices.
Catalogue references include Not applicable.
European nomenclature codes declared: W0104010499, W0104010206, W0104010804, W0104010405, W0104010403, W0104030299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 73 |
| Country of registration | Norway |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 73 |
|---|---|
| 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. Oslo universitetssykehus HF was not found in either the U.S. or the Canadian register.