ME Medical AG
CH-MF-000052198 · Switzerland · Brione sopra Minusio
ME Medical AG is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 11 |
|---|
Among these devices, 1 are declared reusable.
Authorised representative in the Union: KAHLITY France SAS.
Devices declared under this manufacturer
- Clipper SC001 and Charging Station SC005
- Professional Clipper (single)
Catalogue references include SC001, SC001 KIT, SC002, SC004, SC005, SC008.
European nomenclature codes declared: V0199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 11 |
| Country of registration | Switzerland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 11 |
|---|---|
| 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. ME Medical AG was not found in either the U.S. or the Canadian register.