Prolab spółka z ograniczoną odpowiedzialnością
PL-MF-000036482 · Poland · Białystok
Prolab spółka z ograniczoną odpowiedzialnością is registered in the European database on medical devices as a manufacturer, with 29 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 29 |
|---|
Most frequent device types declared: BLOOD TUBE STRIPPER, WARMQUBE Chamber heater.
Among these devices, 24 are declared active.
Devices declared under this manufacturer
- MTS Manual Tube Stripper
- WARMQUBE L Version: C
- WARMQUBE M Version: A
- WARMQUBE M Version: C
- WARMQUBE M Version: D
- WARMQUBE M1 Version: A
- WARMQUBE M1 Version: C
- WARMQUBE M1 Version: D
- WARMQUBE S Version: C
- WARMQUBE S Version: B
- WARMQUBE S Version: D
- WARMQUBE XL Version: A
Showing 12 of 29 declared devices.
Catalogue references include MTS_PRO_MD, PRO-WQ-M1-A-391, PRO-WQ-M1-D-360, PRO-WQ-S-B-025, PRO-WQ-S-C-018, PRO-WQ-S-D-001.
European nomenclature codes declared: Z12019099, B0180.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 29 |
| 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 | 29 |
|---|---|
| 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. Prolab spółka z ograniczoną odpowiedzialnością was not found in either the U.S. or the Canadian register.