numares AG
DE-MF-000022282 · Germany · Regensburg
numares AG is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
Devices declared under this manufacturer
- AXINON® GFR(NMR)
- AXINON® Sample Wizard
- AXINON® Software
- AXINON® System
- AXINON® lipoFIT®
- AXINON® serum kit 2.0 for 100 tests
- AXINON® serum kit 2.0 for 1000 tests
- AXINON® serum kit 2.0 for 20 tests
- AXINON® serum kit 2.0 for 500 tests
Catalogue references include AX0012, AX0028, AX0315-100, AX0315-1000, AX0315-20, AX0315-500.
European nomenclature codes declared: W01010499, W0201010292, W0201010192, W0201010101.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | NUMARES AG (DE) · FDA 3011080315 |
| Devices in EUDAMED | 9 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 9 |
|---|---|
| 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: United States only. numares AG is registered in the United States but was not found in the Canadian register.