Sinclair France SAS
FR-MF-000008945 · France · Lyon
Sinclair France SAS is registered in the European database on medical devices as a manufacturer, with 42 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 42 |
|---|
Most frequent device types declared: Deep, Deep Lidocaine, Derm, Derm Lidocaine, Finelines.
Among these devices, 42 are declared sterile, 42 implantable.
Devices declared under this manufacturer
- Perfectha
- Perfectha Lidocaine
Showing 12 of 42 declared devices.
Catalogue references include PD, PDD, PDDL, PDFL, PDFLL, PDL.
European nomenclature codes declared: X0303.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 42 |
| 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 | 42 |
|---|---|
| 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. Sinclair France SAS was not found in either the U.S. or the Canadian register.