Lifa Air Oy Ltd
FI-MF-000002802 · Finland · Espoo
Lifa Air Oy Ltd is registered in the European database on medical devices as a manufacturer, with 60 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 60 |
|---|
Most frequent device types declared: LM1000, LM2000, LM2000-R.
Devices declared under this manufacturer
- Kirurginen suu-nenäsuojus type I Apteq, 50 kpl
- Lifa Air Medical face mask Type IIR Sunglasses-teddy, 20 pcs
- Lifa Air Medical face mask type I dog, 50 pcs
- Lifa Air Medical face mask type I lilac, 50 pcs
- Lifa Air Medical face mask type I pink, 50 pcs
- Lifa Air Medical face mask type I red, 1 pc
- Lifa Air Medical face mask type IIR Happy person, 20 pcs
- Lifa Air Medical face mask type IIR black, 20 pcs
- Lifa Air Medical face mask type IIR blue, 5 pcs
- Lifa Air Medical face mask type IIR cat, 1 pc
- Lifa Air Medical face mask type IIR cat, 50 pcs
- Lifa Air Medical face mask type IIR red, 50 pcs
Showing 12 of 60 declared devices.
Catalogue references include 6430077230163, 6430077230309, 6430077230385, 6430077230910, 6430077230958, 6430077230996.
European nomenclature codes declared: T020604, T020603.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 60 |
| 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 | 60 |
|---|---|
| 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. Lifa Air Oy Ltd was not found in either the U.S. or the Canadian register.