REVITACARE SAS
FR-MF-000004021 · France · Saint Ouen l'Aumone
REVITACARE SAS is registered in the European database on medical devices as a manufacturer, with 17 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 17 |
|---|
Among these devices, 17 are declared sterile, 17 implantable.
Devices declared under this manufacturer
- CYTOCARE 502
- CYTOCARE 516
- CYTOCARE 532
- CYTOCARE S Line
- DERMASTIR 16 EBF
- DERMASTIR 32 EBF
- DERMASTIR H13
- HAIRCARE
- REVITAFILL Essential 1
- REVITAFILL Essential 2
- REVITAFILL Essential 3
- REVITAFILL Essential 4
Showing 12 of 17 declared devices.
Catalogue references include CT532/5, CTSL, CY516, CY516/5, CZ502, DE3/5.
European nomenclature codes declared: X0301, X0303.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 17 |
| 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 | 17 |
|---|---|
| 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. REVITACARE SAS was not found in either the U.S. or the Canadian register.