Medicom SAS
FR-MF-000002873 · France · Saint Barthélemy d'Anjou
Medicom SAS is registered in the European database on medical devices as a manufacturer, with 286 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 286 |
|---|
Most frequent device types declared: TIIR & FFP2 NR D Mask, TIIR & FFP3 NR D Mask.
Devices declared under this manufacturer
- Feeldry
- Omnimask Comfort
- Op Air
- Op Air One
- Premium Face Mask
- SafeDrape
- SafeMatrix
- SafeTouch 400
- SafeTouch Black Lite
- SafeTouch Long
- SafeTouch Rejuvenate
- SafeTouch Slim
Showing 12 of 286 declared devices.
Catalogue references include 1121-D, 1175N-A, 441885, 441888, M31201-30, M34101-40.
European nomenclature codes declared: T020604, T01020204, T010201, T0208, T0207, S01010101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 286 |
| 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 | 286 |
|---|---|
| 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. Medicom SAS was not found in either the U.S. or the Canadian register.