Maxeta AS
NO-MF-000015725 · Norway · Skien
Maxeta AS 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 |
|---|
Most frequent device types declared: P201-100, P201-125, P201-170, P201-215, P203-268.
Catalogue references include P201-100, P201-125, P201-170, P201-215, P203-268, P203-374.
European nomenclature codes declared: Z120309.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| 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 | 6 |
|---|---|
| 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. Maxeta AS was not found in either the U.S. or the Canadian register.