Vitberg Sikora Jacek
PL-MF-000010936 · Poland · Nowy Sącz
Vitberg Sikora Jacek is registered in the European database on medical devices as a manufacturer, with 19 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 19 |
|---|
Most frequent device types declared: Moduł RS2, RS2.
Among these devices, 15 are declared active.
Devices declared under this manufacturer
- Klin Pozycjonujący 1 RS2
- Klin Pozycjonujący 2 RS2
- Klin Pozycjonujący 3 RS2
- Moduł Nogi RS2
- Podłokietniki RS2
- Vitberg Recovery System - Aparat Bazowy RS2
- Vitberg Recovery System - Aparat Bazowy RS2 (Aparat rehabilitacyjny V2
- Vitberg Recovery System - Moduł Brzuch RS2 (Moduł rehabilitacyjny V2MF
- Vitberg Recovery System - Moduł Kolana RS2 (Moduł rehabilitacyjny V2MB
- Vitberg Recovery System - Moduł Plecy RS2 (Moduł rehabilitacyjny V2MDS
- Vitberg Recovery System - Moduł Ręce RS2 (Moduł rehabilitacyjny V2MGKP
- Vitberg Recovery System - Moduł Ręce RS2 (Moduł rehabilitacyjny V2MGSP
Showing 12 of 19 declared devices.
Catalogue references include V2ABSP, V2K1S, V2K2S, V2K3S, V2MAS, V2MGS.
European nomenclature codes declared: Z120616, V080302.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 19 |
| 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 | 18 |
|---|---|
| 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. Vitberg Sikora Jacek was not found in either the U.S. or the Canadian register.