Sensotrend Oy
FI-MF-000000500 · Finland · Tampere
Sensotrend Oy is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 8 |
|---|
Most frequent device types declared: Sensotrend Connect Carelink, diabetes-dossier.ch AGP Bericht, diabetes-dossier.ch Connect, diabetes-dossier.ch Uploader.
Among these devices, 8 are declared active.
Devices declared under this manufacturer
- Nightscout Connect
- Sensotrend Connect
- Sensotrend Connect Carelink
- Sensotrend Dashboard
- Sensotrend Uploader
- diabetes-dossier.ch AGP Bericht
- diabetes-dossier.ch Connect
- diabetes-dossier.ch Uploader
Catalogue references include SC000001, SCC00001, SCP00001, SD000001, SDP00001, SU000001.
European nomenclature codes declared: V92.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| Country of registration | Finland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
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. Sensotrend Oy was not found in either the U.S. or the Canadian register.