Kajo Apuvälineet Oy
FI-MF-000002471 · Finland · Tampere
Kajo Apuvälineet Oy is registered in the European database on medical devices as a manufacturer, with 20 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 20 |
|---|
Most frequent device types declared: KB25 KB50 KB100 KSB80, Kajo Kymppi.
Devices declared under this manufacturer
- KB100
- KB25
- KB50
- KSB80
- Kajo Kymppi
Showing 12 of 20 declared devices.
Catalogue references include KB100 250CB, KB25 100BB, KB25 150AB, KB25 150BB, KB50 150AB, KB50 150BB.
European nomenclature codes declared: Y240999, Y214209.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 20 |
| 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 | 20 |
|---|---|
| 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. Kajo Apuvälineet Oy was not found in either the U.S. or the Canadian register.