TECINSOM
FR-MF-000040495 · France · PAU
TECINSOM is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 6 |
|---|
Devices declared under this manufacturer
- Bouillotte Cervicale Pur Lin
- Bouillotte Enfant Pur Lin
- Bouillotte Ophtalmique Pur Lin
- Bouillotte lombaire Pur Lin
Catalogue references include Bouillotte Cervicale Pur Lin, Bouillotte Enfant Pur Lin, Bouillotte de thermothérapie Beauty Face, Bouillotte de thermothérapie Ophtalmique, Bouillotte de thermothérapie Serpentin, Bouillotte lombaire Pur Lin.
European nomenclature codes declared: M9001.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
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: Neither register. TECINSOM was not found in either the U.S. or the Canadian register.