M Prekyba UAB
LT-MF-000022623 · Lithuania · Siauliai
M Prekyba UAB is registered in the European database on medical devices as a manufacturer, with 12 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 12 |
|---|
Most frequent device types declared: BETA, IMO100, JUPITER 16, JUPITER 20, ORTO.
Among these devices, 1 are declared active.
Devices declared under this manufacturer
- BETA
- IMO100
- JUPITER 16
- JUPITER 18
- JUPITER 20
- ORTO
- ORTO PLUS
- PR1000
- SATURN XL
Catalogue references include 20, IMO100, JUPITER 18, JUPITER 20, ORTO 200x90x12 cm, ORTO PLUS 200x85x12 cm.
European nomenclature codes declared: Y122106, V080702, Y093312, V08060101, V08068099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 12 |
| Country of registration | Lithuania |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 12 |
|---|---|
| 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. M Prekyba UAB was not found in either the U.S. or the Canadian register.