BANO Healthcare GmbH
AT-MF-000000742 · Austria · Baden
BANO Healthcare GmbH is registered in the European database on medical devices as a manufacturer, with 15 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 15 |
|---|
Devices declared under this manufacturer
- SILVERIN® STICKS 50% 115mm elastisch 100Stk.
- SILVERIN® STICKS 50% 115mm elastisch 10Stk.
- SILVERIN® STICKS 50% 115mm starr 100Stk.
- SILVERIN® STICKS 50% 115mm starr 10Stk.
- SILVERIN® STICKS 50% 200mm elastisch 10Stk.
- SILVERIN® STICKS 50% 200mm starr 100Stk.
- SILVERIN® STICKS 50% 200mm starr 10Stk.
- SILVERIN® STICKS 75% 115mm elastisch 100Stk.
- SILVERIN® STICKS 75% 115mm starr 100Stk.
- SILVERIN® STICKS 75% 200mm starr 100Stk.
- SILVERIN® STICKS 75% 200mm starr 10Stk.
- SILVERIN® STÄBCHEN 50% 115mm elastisch 10Stk.
Showing 12 of 15 declared devices.
Catalogue references include 1304124, 1304148, 1304155, 1304162, 1304179, 1304230.
European nomenclature codes declared: Q030299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 15 |
| Country of registration | Austria |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 15 |
|---|---|
| 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. BANO Healthcare GmbH was not found in either the U.S. or the Canadian register.