Kinesis Spółka z ograniczoną odpowiedzialnością
PL-MF-000023594 · Poland · Miejsce Piastowe
Kinesis Spółka z ograniczoną odpowiedzialnością is registered in the European database on medical devices as a manufacturer, with 54 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 54 |
|---|
Most frequent device types declared: Fotel ginekologiczny, PS-K, Stolik do badań niemowląt.
Among these devices, 8 are declared active.
Devices declared under this manufacturer
- Kozetka lekarska KZ
- Kozetka lekarska KZ-CH
- Kozetka lekarska KZ2
- Linka 60cm ST4
- PERFECT G
- Schody do nauki chodzenia
- Schody do nauki chodzenia z pochylnią
- Stolik ELEGANT
- Stolik ST
- Stolik do EKG
- Stolik do badań niemowląt KS1
- Tor do nauki chodzenia bez przeszkód
Showing 12 of 54 declared devices.
Catalogue references include GYMNESIS CIRCLE L, KLD3, KZ-CH, KZ2, OSPRZĘT STANDARD, Sling Therapy KINESIS Standard.
European nomenclature codes declared: Z120602, Y050202, Y050201, Z12069099, V080202, Y0503.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 54 |
| Country of registration | Poland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 54 |
|---|---|
| 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. Kinesis Spółka z ograniczoną odpowiedzialnością was not found in either the U.S. or the Canadian register.