UAB Pirmas žingsnis
LT-MF-000004764 · Lithuania · Kaunas
UAB Pirmas žingsnis is registered in the European database on medical devices as a manufacturer, with 37 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 37 |
|---|
Most frequent device types declared: PKA311, SAP11, SAP12, SKA562, SKA563.
Devices declared under this manufacturer
- PKA311
- SAP11
- SAP12
- SKT514
- SRL14
- SSK11
- SSK13
- SSK42
Showing 12 of 37 declared devices.
Catalogue references include 6, 8, 9, TD/108, TD/115, TD/124.
European nomenclature codes declared: Y061209, M03050299, Y061219, Y06120601.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 37 |
| 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 | 37 |
|---|---|
| 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. UAB Pirmas žingsnis was not found in either the U.S. or the Canadian register.