Jabbla
BE-MF-000049893 · Belgium · Gent
Jabbla is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 6 |
|---|
Most frequent device types declared: Tellus.
Devices declared under this manufacturer
- Allora 3
- HeyPad
- Tellus 6
- Tellus i6
- Vibe 10
- Vibe 12+
Catalogue references include A3-2855, HP-3203, T6-2632, T6-2633, VP-2979, VX-2753.
European nomenclature codes declared: Y214212.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | JABBLA (BE) · FDA 3007275470 |
| Devices in EUDAMED | 6 |
| Country of registration | Belgium |
Device-level evidence
| Devices with a numeric GTIN | 6 |
|---|---|
| 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: United States only. Jabbla is registered in the United States but was not found in the Canadian register.