ELLIPSE
FR-MF-000023841 · France · Roubaix
ELLIPSE is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 9 |
|---|
Devices declared under this manufacturer
- Crème adhésive pour appareils dentaires
- Crème fixative pour appareils dentaire - tolérance & confort
- Crème fixative pour appareils dentaires Fraîcheur
- Crème fixative pour appareils dentaires classique
- Crème fixative pour appareils dentaires hypoallergénique
- Crème fixative pour prothèses dentaires
Catalogue references include CPSF - 1088, CPSF - 1156, CPSF 851, CPSF 852, CPSF-119, CPSF-570.
European nomenclature codes declared: P01020180.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| 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 | 9 |
|---|---|
| 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. ELLIPSE was not found in either the U.S. or the Canadian register.