MEDISTAR
FR-MF-000042737 · France · Nice
MEDISTAR is registered in the European database on medical devices as a manufacturer, with 139 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 139 |
|---|
Devices declared under this manufacturer
- Kit patient ambulatoire Eco taille 2XL
- Kit patient ambulatoire spécifique - Taille Adulte
- Kit patient peignoir - Taille Adulte
- Kit patient spécifique - Taille Adulte
- Kit patient spécifique - Taille XL
- Peignoir bleu - Taille 5XL
- Pyjama CONFORT+ parme - Taille 3XL
- Pyjama CONFORT+ parme - Taille L
- Pyjama CONFORT+ parme - Taille M
- Pyjama CONFORT+ rose - Taille XL
- Pyjama ECO+ bleu - Taille 2XL
- Pyjama ECO+ vert - Taille L
Showing 12 of 139 declared devices.
Catalogue references include 7030EN, 7539B, 7596, 7705, 7709-3XL, 7722.
European nomenclature codes declared: T0299, T030502, T0205, T020604, T0208, T0207.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 139 |
| 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 | 139 |
|---|---|
| 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. MEDISTAR was not found in either the U.S. or the Canadian register.