2ingis
BE-MF-000020999 · Belgium · Bruxelles
2ingis is registered in the European database on medical devices as a manufacturer, with 55 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 55 |
|---|
Devices declared under this manufacturer
- Caps 3.0 NSK
- Caps 3.0 W&H
- Legs 5.1 Long
- Legs 5.1 Short
- Sapcer 4.0 6,5
- Spacer 4.0 10,0
- Spacer 4.0 2,0
- Spacer 4.0 2,5
- Spacer 4.0 3,0
- Spacer 4.0 4,0
- Spacer 4.0 4,5
- Spacer 4.0 5,0
Showing 12 of 55 declared devices.
Catalogue references include NSMDI, ZA320RG, ZA525RG, ZA550RG, ZA600RG, ZG551IT.
European nomenclature codes declared: L80.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 55 |
| Country of registration | Belgium |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 55 |
|---|---|
| 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. 2ingis was not found in either the U.S. or the Canadian register.