Innoforce Anstalt
LI-MF-000002047 · Liechtenstein · Ruggell
Innoforce Anstalt is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 11 |
|---|
Among these devices, 11 are declared active.
Devices declared under this manufacturer
- ENTstatistics
Catalogue references include ECM 5.1, ECM 5.1.19, ENTstatistics 5.1.18, IFDM 5.1, IFDM 5.1.18, IFDM 5.1.19.
European nomenclature codes declared: V92,Z12129092, V92,Z12149092, V92,Z12129092,Z12149092.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 11 |
| Country of registration | Liechtenstein |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 2 |
|---|---|
| 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. Innoforce Anstalt was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
Z-24-137-S-IX | issued | 2030-08-14 |