Med & Life Sp. z o.o.
PL-MF-000024639 · Poland · Komorów
Med & Life Sp. z o.o. is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 9 |
|---|
Among these devices, 9 are declared active.
Devices declared under this manufacturer
- Viofor JPS System Delux
- Viofor JPS System Family
- Viofor JPS System Family +
- Viofor JPS System Family Plus
- Viofor JPS System MagneticLight
- Viofor JSP System Classic
- Viofor S
- Viofor S-Pro
Catalogue references include REF 1031, REF 1035, REF 1036, REF 1037, REF 1038, REF 1039.
European nomenclature codes declared: Z12040202,Z120606, Z120606.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| 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 | 9 |
|---|---|
| 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. Med & Life Sp. z o.o. was not found in either the U.S. or the Canadian register.