Glamox AS
NO-MF-000052034 · Norway · Molde
Glamox AS is registered in the European database on medical devices as a manufacturer, with 91 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 91 |
|---|
Among these devices, 91 are declared active.
Catalogue references include Circus LED (M) T100 AWh 600 940 3,5D CLA BT NA, CircusLEDMT100Wh6009405DCLA DK, LHH G2 C105 AWh 1300 940 P BT NA, LHH G2 C105 AWh 900 935-945 CCT BT NA, LHH G2 C105 AWh 900 935-945 CCT P AU, LHH G2 T105 AWh 1300 940 TR P GB.
European nomenclature codes declared: Z120499.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 91 |
| 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 | 91 |
|---|---|
| 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. Glamox AS was not found in either the U.S. or the Canadian register.