Aether Biomedical Spółka z ograniczoną odpowiedzialnością
PL-MF-000005368 · Poland · Poznan
Aether Biomedical Spółka z ograniczoną odpowiedzialnością is registered in the European database on medical devices as a manufacturer, with 17 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 17 |
|---|
Most frequent device types declared: A-01-L, A-01-L-T, A-01-L-TS-S, A-01-R, A-01-R-T.
Among these devices, 17 are declared active.
Devices declared under this manufacturer
- Aether Battery System
- Aether MyoSense
- ZEUS
- Zeus
Showing 12 of 17 declared devices.
Catalogue references include A-01-R Zeus V 1, A02L-SF0B, A02L-SF1B, A02R-SF0B, A02R-SF1B, AET-BAT-BS1.
European nomenclature codes declared: Y061899, Y240999.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 17 |
| Country of registration | Poland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 17 |
|---|---|
| Found in the U.S. device database | 7 |
| Share | 41.2 % |
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. Aether Biomedical Spółka z ograniczoną odpowiedzialnością was not found in either the U.S. or the Canadian register.