SANKOM SA
CH-MF-000047525 · Switzerland · Delemont
SANKOM SA is registered in the European database on medical devices as a manufacturer, with 74 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 74 |
|---|
Most frequent device types declared: SANKOM Patent Tights.
Among these devices, 1 are declared sterile.
Authorised representative in the Union: Roberto Sanchez Beltran.
Devices declared under this manufacturer
- Avevitta
- SANKOM
- SANKOM Tights Beige L-XL
- SANKOM Tights Beige S-M
- SANKOM Tights Beige XXL
- SANKOM Tights Black L-XL
- SANKOM Tights Black S-M
- SANKOM Tights Black XXL
Showing 12 of 74 declared devices.
Catalogue references include SAN-040DB Dark Blue L-XL, SAN-040GRS-M, SAN-040WT White L-XL, SAN-091TBL Black L-XL, SAN-091TBL Black XXL, SAN-121BG Beige Belt S-M.
European nomenclature codes declared: M030499, M030405, Y060399, T04010103.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 74 |
| 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 | 74 |
|---|---|
| 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. SANKOM SA was not found in either the U.S. or the Canadian register.