Viacell s.r.o.
CZ-MF-000051827 · Czechia · Ústí nad Labem
Viacell s.r.o. is registered in the European database on medical devices as a manufacturer, with 35 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 35 |
|---|
Most frequent device types declared: Náplasti cívkové, Náplasti s polštářkem.
Among these devices, 1 are declared sterile.
Devices declared under this manufacturer
- BABYPORE
- VIACELL C120E
- VIACELL C121
- VIACELL C141MIX
- VIACELL CN342
- VIACELL D121B
- VIACELL D123FE
- VIACELL F131
- VIACELL F143
- VIACELL M121
- VIACELL M141
- VIACELL M156
Showing 12 of 35 declared devices.
Catalogue references include 1019.04, 1037.04, 1041.04, 1102.04, 1117.04, 1209.04.
European nomenclature codes declared: M04010199, M050101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 35 |
| Country of registration | Czechia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 35 |
|---|---|
| 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. Viacell s.r.o. was not found in either the U.S. or the Canadian register.