Dimea Oy
FI-MF-000039392 · Finland · Turku
Dimea Oy is registered in the European database on medical devices as a manufacturer, with 77 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 77 |
|---|
Devices declared under this manufacturer
- Tarume Adventure
- Tarume Boss lady
- Tarume Lovestory
- Tarume Petit
- Tarume Rainbow
- Tarume Shine
- Tarume The Author
- Tarume Wink
- Tarume You Rock!
- Tarume art 11a
- Tarume art 12a
- Tarume art 14a
Showing 12 of 77 declared devices.
Catalogue references include 06430082120060, 06430082120206, 06430082120220, 06430082120268, 06430082120381, 06430082120602.
European nomenclature codes declared: Q02100202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 77 |
| Country of registration | Finland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 77 |
|---|---|
| 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. Dimea Oy was not found in either the U.S. or the Canadian register.