GRASO Zenon Sobiecki
PL-MF-000022437 · Poland · Starogard Gdański
GRASO Zenon Sobiecki is registered in the European database on medical devices as a manufacturer, with 384 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- Brain Heart Infusion (BHI) Broth
- CHROMagar MRSA
- CHROMagar Serratia
- Columbia Agar + 5% Sheep Blood
- Gardenella Vaginalis Agar +5% Horse Blood
- Hektoen Enteric Agar
- Mannitol Salt Agar (Chapman Medium)
- Meningomedium Plus
- Mueller Hinton II Agar
- PP Red Agar
- Selenite F Broth
- Tryptic Soy Agar (TSA) + 5% Sheep Blood
Showing 12 of 384 declared devices.
Catalogue references include 1041PD90, 1050PD90, 1190PD140, 1280PD90, 201402, 3037BT200(KG).
European nomenclature codes declared: W0104010405, W0104010206, W0104010306, W0104010206,W0104080299, W0104010306,W0104080299, W0104010407.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 384 |
| 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 | 384 |
|---|---|
| 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. GRASO Zenon Sobiecki was not found in either the U.S. or the Canadian register.