VELECO Sp z o.o
PL-MF-000026289 · Poland · Częstochowa
VELECO Sp z o.o is registered in the European database on medical devices as a manufacturer, with 14 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 14 |
|---|
Most frequent device types declared: COSMO, DRACO, FLEXO ALUMINIUM, FLEXO CARBON, GRAVIS.
Among these devices, 12 are declared active.
Catalogue references include 05904553994234, 05904553994241, 05904553994272, 05904553994289, 05904553994296, 05905525308004.
European nomenclature codes declared: Y122124, Y120606, Y122127.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 14 |
| 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 | 14 |
|---|---|
| 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. VELECO Sp z o.o was not found in either the U.S. or the Canadian register.