Solift, s.r.o.
CZ-MF-000055130 · Czechia · Brno
Solift, s.r.o. is registered in the European database on medical devices as a manufacturer, with 13 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 13 |
|---|
Among these devices, 12 are declared active.
Devices declared under this manufacturer
- soline® bibi battery
- soline® bibi mobile
- soline® bibi safety
- soline® bibi standard
- soline® lara E
- soline® lara H
- soline® leny
- soline® lucy E
- soline® lucy EW
- soline® marco E
- soline® marco H
- soline® tiby E
Showing 12 of 13 declared devices.
Catalogue references include 001, 004, 005, 008, 009, 010.
European nomenclature codes declared: Y093399, Y091209, V08050101, Y093312.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 13 |
| 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 | 13 |
|---|---|
| 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. Solift, s.r.o. was not found in either the U.S. or the Canadian register.