Pulmeq sp. z o.o.
PL-MF-000029225 · Poland · Gorzów Wielkopolski
Pulmeq sp. z o.o. is registered in the European database on medical devices as a manufacturer, with 13 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 13 |
|---|
Most frequent device types declared: PQFS-28, PQFS-30, PQFS-30S, PQUS-20, PQUS-22.
Devices declared under this manufacturer
- Jednorazowe kształtki z pianki
- Jednorazowy filtr do badań spirometrycznych
- Jednorazowy klips na nos
- Jednorazowy ustnik do spirometru
- Klips na nos
Showing 12 of 13 declared devices.
Catalogue references include PQFS-28, PQFS-30S, PQUS-20, PQUS-22, PQUS-26, PQUS-28.
European nomenclature codes declared: Z12150185.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 13 |
| 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 | 13 |
|---|---|
| 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. Pulmeq sp. z o.o. was not found in either the U.S. or the Canadian register.