PRO-PROJECT GROUP SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ
PL-MF-000031595 · Poland · Lublin
PRO-PROJECT GROUP SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ is registered in the European database on medical devices as a manufacturer, with 48 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 48 |
|---|
Devices declared under this manufacturer
- PRO-PROJECT ProNM ACR Performance SPECT + PET
- ProCT Align
- ProCT ProVet
- ProCT mk II
- ProHVL
- ProMAM AEC PMMA
- ProMAM Accreditation
- ProMRI
- ProNM Performance
- ProNM Resolution
- ProRTG AEC Cu
- ProRTG AEC PMMA
Showing 12 of 48 declared devices.
Catalogue references include PRO-PROJECT ProNM ACR Performance SPECT + PET, Pro-HVL, Pro-MRI, Pro-NM Resolution, Pro-RTG AEC Cu, Pro-RTG AEC PMMA.
European nomenclature codes declared: V0399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 48 |
| 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 | 48 |
|---|---|
| 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. PRO-PROJECT GROUP SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ was not found in either the U.S. or the Canadian register.