Mego Pro s.r.o.
CZ-MF-000042344 · Czechia · Praha 8
Mego Pro s.r.o. is registered in the European database on medical devices as a manufacturer, with 25 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 25 |
|---|
Most frequent device types declared: MP2040, MP2086, MP2092, MP4161, MP4169.
Devices declared under this manufacturer
- MP2040
- MP2086
- MP2087
- MP2092
- MP4161
- MP4169
- MP4170
- MP6228
- MP6234
- MP6242
- MP6245
- MP6246
Showing 12 of 25 declared devices.
Catalogue references include MP2040, MP2086, MP2092, MP4161, MP6228, MP6246.
European nomenclature codes declared: Y210399, Q0210030299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 25 |
| Country of registration | Czechia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 25 |
|---|---|
| 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. Mego Pro s.r.o. was not found in either the U.S. or the Canadian register.