Filterpak Oy Ab Ltd
FI-MF-000007331 · Finland · Hanko
Filterpak Oy Ab Ltd is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 9 |
|---|
Most frequent device types declared: NeSu Type II, NeSuTypeIIR3W.
Devices declared under this manufacturer
- Nesu Professional Black-Edition, type II
- Nesu Professional Black-Edition, type IIR
- Nesu Professional Blue-Edition, type II
- Nesu Professional Blue-Edition, type IIR
- Nesu Professional Pink-Edition, type II
- Nesu Professional Pink-Edition, type IIR
- Nesu Professional UltraSoft -face mask, type II
- Nesu Professional White-Edition, type II
- Nesu Professional White-Edition, type IIR
Catalogue references include 06430078970006, 06430078970013, 06430078970020, 06430078970037, 06430078970044, 06430078970068.
European nomenclature codes declared: T020604.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| Country of registration | Finland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 9 |
|---|---|
| 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. Filterpak Oy Ab Ltd was not found in either the U.S. or the Canadian register.