BEMER Int. AG
LI-MF-000002555 · Liechtenstein · Triesen
BEMER Int. AG is registered in the European database on medical devices as a manufacturer, with 20 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 20 |
|---|
Among these devices, 17 are declared active.
Devices declared under this manufacturer
- B.Bed Evo
- B.Body Classic
- B.Body Evo
- B.Body Professional
- B.Box Classic
- B.Box Evo
- B.Grip
- B.Light
- B.Light Clear Evo
- B.Light Restore Evo
- B.Pad
- B.Spot
Showing 12 of 20 declared devices.
Catalogue references include 420100, 430100, 430200, 430300, 431000, 431100.
European nomenclature codes declared: Z12062801, Z12040202, A070199, Z12040203.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | BEMER Int. AG (LI) · FDA 3009102830 |
| Devices in EUDAMED | 20 |
| Country of registration | Liechtenstein |
Device-level evidence
| Devices with a numeric GTIN | 20 |
|---|---|
| Found in the U.S. device database | 10 |
| Share | 50.0 % |
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. BEMER Int. AG is registered in the United States but was not found in the Canadian register.