Calpro AS
NO-MF-000036194 · Norway · Lysaker
Calpro AS is registered in the European database on medical devices as a manufacturer, with 10 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: CAL0510, CAL0510L, CAL201, CAL230, CAL240, CAL250.
Devices declared under this manufacturer
- CalproSmart Self-Test
- EasyExtract
- Lyfstone Calprotectin for Synovial Fluid
Catalogue references include CAL0510, CAL0510L, CAL201, CAL220, CAL230, CAL250, CALP0170.
European nomenclature codes declared: W0102100899, W0102019009, W01010699, W0101060399, W0102160699, W05019001.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 10 |
| 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 | 10 |
|---|---|
| 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. Calpro AS was not found in either the U.S. or the Canadian register.