Segetex-eif
FR-MF-000007669 · France · Ivry-sur-Seine
Segetex-eif is registered in the European database on medical devices as a manufacturer, with 44 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 44 |
|---|
Devices declared under this manufacturer
- Pyjama ColorSoft Bleu Taille XS
- Pyjama SegeSoft Bleu Taille S
- Pyjama SegeSoft Bleu Taille XL
- Pyjama SegeSoft Bleu Taille XXL
- Pyjama SegeSoft Parme Taille M
- Pyjama SegeSoft Parme Taille S
- Pyjama SegeSoft Parme Taille XXL
- Pyjama SegeSoft Prune Taille M
- Pyjama SegeSoft Rose Taille L
- Pyjama SegeSoft Rose Taille S
- Pyjama SegeSoft Vert Taille L
- Pyjama SegeSoft Vert Taille M
Showing 12 of 44 declared devices.
Catalogue references include M212-50BE, M212-50PM, M212-50VT, M213-50PR, M213-50VT, M214-50RO.
European nomenclature codes declared: T0205, T0299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 44 |
| 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 | 44 |
|---|---|
| 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. Segetex-eif was not found in either the U.S. or the Canadian register.