Lumatix s.r.o.
SK-MF-000005675 · Slovakia · Bratislava
Lumatix s.r.o. is registered in the European database on medical devices as a manufacturer, with 56 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 56 |
|---|
Most frequent device types declared: A40, FRONT, H20, SPORT100, T45.
Devices declared under this manufacturer
- Medicovi A40 ortopedické vložky 36-37
- Medicovi A40 ortopedické vložky 46-47
- Medicovi Front ortopedické vložky 34-35
- Medicovi H20 ortopedické vložky 38-39
- Medicovi H20 ortopedické vložky 46-47
- Medicovi Sport 100 ortopedické vložky 36-37
- Medicovi Sport 100 ortopedické vložky 40-41
- Medicovi Sport 100 ortopedické vložky 46-47
- Medicovi T40 ortopedické vložky 36-37
- Medicovi T40 ortopedické vložky 46-47
- Medicovi T45 ortopedické vložky 38-39
- Medicovi T45 ortopedické vložky 46-47
Showing 12 of 56 declared devices.
Catalogue references include MA404647, MFRT3435, MH203839, MS103637, MS104041, MT404647.
European nomenclature codes declared: Y061203.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 56 |
| Country of registration | Slovakia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 56 |
|---|---|
| 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. Lumatix s.r.o. was not found in either the U.S. or the Canadian register.