UAB Kasko Group
LT-MF-000007721 · Lithuania · Vilnius
UAB Kasko Group is registered in the European database on medical devices as a manufacturer, with 83 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 83 |
|---|
Most frequent device types declared: GIGAS, KID-MAN, LIGHTMAN COMFORT PLUS XL, LIGHTMAN TRAVEL, LIGTHTMAN START.
Devices declared under this manufacturer
- 02-8015C
- FARGO
- GIGAS
- KID-MAN
- LIGHTMAN COMFORT PLUS XL
- LIGHTMAN START
- LIGHTMAN START PLUS
- LIGHTMAN TRAVEL
- LIGTHTMAN START
- MEGO
- SITIS
- STEELMAN START
Showing 12 of 83 declared devices.
Catalogue references include 01-3530, 01-3540, 02-7060L6, 04-030-2/54, 04-035-3/51, 04-055-3/44.
European nomenclature codes declared: Y122106, T01020204, Y122103, Y120606, T01020201, Y120399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 83 |
| 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 | 83 |
|---|---|
| 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 Kasko Group was not found in either the U.S. or the Canadian register.