PZ CORMAY Spółka Akcyjna
PL-MF-000023053 · Poland · Łomianki
PZ CORMAY Spółka Akcyjna is registered in the European database on medical devices as a manufacturer, with 721 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| other | 721 |
|---|
Most frequent device types declared: PRESTIGE 24i LQ MG, PRESTIGE 24i COMPLEMENT C3, PRESTIGE 24i URINE PROTEINS, AURYX 90 HE4 Reagent Kit, AURYX 90 CK-MB Reagent Kit.
No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 721 |
| Country of registration | Poland |
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.