KOLASA SPÓŁKA JAWNA
PL-MF-000044993 · Poland · Łódź
KOLASA SPÓŁKA JAWNA is registered in the European database on medical devices as a manufacturer, with 285 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- Bufor rozcieńczający barwnik Giemsy stężony 20x 500ml
- Błękit metylenowy Loefflera 1L
- Cytrynian trisodowy 3,8% 1L
- Formaldehyd 10% buforowany (Utrwalacz do badań histologicznych) 5L
- Formaldehyd 10% stabilizowany (Utrwalacz do badań histologicznych) 5kg
- Formaldehyd 37% (do badań histologicznych) 5kg
- Formalina buforowana 10% Stężenie formaldehydu 4% (Utrwalacz do badań
- Fuksyna karbolowa (do barwienia metodą Ziehl-Neelsena „na zimno”) 1L
- HP-C Alkohol etylowy 99,9% (skażony) 1L
- Odczynnik Ehrlicha 500ml
- Odczynnik LISS 100ml
- Odczynnik Lugola (roztwór do barwienia metodą Grama) 1L
Showing 12 of 285 declared devices.
Catalogue references include 1062.3, 2005.2, 2088.2, 3030.5, 3421.4, 3423.41.
European nomenclature codes declared: W01030705, W0104010804, W01030799, W0103010302, W0103010301, W01030199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 285 |
| 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 | 285 |
|---|---|
| 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. KOLASA SPÓŁKA JAWNA was not found in either the U.S. or the Canadian register.