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
Most frequent device types declared: ACCENT-200 LIPOPROTEIN (a), AURYX 90 CK-MB Reagent Kit, AURYX 90 HE4 Reagent Kit, CORMAY Lp (a) CONTROL N, HC-UREA.
Devices declared under this manufacturer
- A-800 URINE PROTEINS
- ACCENT-200 LIPOPROTEIN (a)
- ACCENT-200 PHOSPHORUS
- AURYX 90 CK-MB Reagent Kit
- AURYX 90 HE4 Reagent Kit
- CORMAY Lp (a) CONTROL N
- HC-UREA
- Liquick Cor-ASAT 30
- Liquick Cor-CREATININE 30
- Liquick Cor-UA 120
- OS-MICROALBUMIN
- PRESTIGE 24i COMPLEMENT C3
Showing 12 of 721 declared devices.
Catalogue references include 2-209, 4-242, 4-335, 4-492, 7-228, 9-463.
European nomenclature codes declared: W01010203, W01010207, W01010213, W01010230, W01010107, W0201010185.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 721 |
| 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 | 721 |
|---|---|
| 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. PZ CORMAY Spółka Akcyjna was not found in either the U.S. or the Canadian register.