LB BOHEMIA, s.r.o.
CZ-MF-000051784 · Czechia · Břeclav
LB BOHEMIA, s.r.o. is registered in the European database on medical devices as a manufacturer, with 26 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 26 |
|---|
Devices declared under this manufacturer
- BOHEMIA CLINIC FLEX
- BOHEMIA CLINIC NEO FLEX
- BOHEMIA ERGONOMIC NEO
- BOHEMIA ERGONOMIC NEO FLEX
- BOHEMIA EUCATHERM FLEX
- BOHEMIA EULASTIC FLEX
- BOHEMIA LUX
- BOHEMIA LUX DUO
- BOHEMIA LUX DUO FLEX
- BOHEMIA LUX FLEX
- BOHEMIA LUXURA NEO
- BOHEMIA LUXURA NEO FLEX
Showing 12 of 26 declared devices.
European nomenclature codes declared: V080702.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 26 |
| 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 | 26 |
|---|---|
| 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. LB BOHEMIA, s.r.o. was not found in either the U.S. or the Canadian register.