TiMask Suisse Sagl
CH-MF-000025278 · Switzerland · Ligornetto
TiMask Suisse Sagl is registered in the European database on medical devices as a manufacturer, with 98 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 98 |
|---|
Most frequent device types declared: Mascherine chirurgiche, TIME, FFP2 NR.
Authorised representative in the Union: UKALIA Limited.
Devices declared under this manufacturer
- KIDS Mascherine chirurgiche con elastici
- Mascherina monouso FFP2 NR
- Mascherine chirurgiche con elastici
Showing 12 of 98 declared devices.
Catalogue references include 20204, 20227, 30203, 30205, 50210, 50211.
European nomenclature codes declared: T020604, T020699, T0205, T0207.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 98 |
| 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 | 98 |
|---|---|
| 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. TiMask Suisse Sagl was not found in either the U.S. or the Canadian register.