Incereb Ltd
IE-MF-000002463 · Ireland · Dublin
Incereb Ltd is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 7 |
|---|
Most frequent device types declared: TF01, TF01K, TF04, TF04K, TF09.
Devices declared under this manufacturer
- Neon 12
- Neon 8
- Neon12
- Neon8
Catalogue references include TF01, TF01-IT, TF01K, TF04, TF04-IT, TF04K.
European nomenclature codes declared: N01010299, N01010202.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | INCEREB LTD (IE) · FDA 3004695199 |
| Devices in EUDAMED | 7 |
| Country of registration | Ireland |
Device-level evidence
| Devices with a numeric GTIN | 7 |
|---|---|
| Found in the U.S. device database | 5 |
| Share | 71.4 % |
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. Incereb Ltd is registered in the United States but was not found in the Canadian register.