Viking Lab Oy
FI-MF-000005746 · Finland · Ylöjärvi
Viking Lab Oy is registered in the European database on medical devices as a manufacturer, with 12 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 12 |
|---|
Most frequent device types declared: BF1003, BF1005, BF1006, BF1009, BF2003.
Devices declared under this manufacturer
- BIOFROST ACTIVE 100ML
- BIOFROST ACTIVE 3ML
- BIOFROST ACTIVE 500ML
- BIOFROST ACTIVE 75ML
- BIOFROST RELIEF 100ML
- BIOFROST RELIEF 3ML
- BIOFROST RELIEF 500ML
- BIOFROST RELIEF 75ML
- NORDALYN 100ml
- NORDALYN 3ml
- NORDALYN 500ml
- NORDALYN 75ml
Catalogue references include BF1003, BF1005, BF1006, BF1009, BF2003, BF2005.
European nomenclature codes declared: V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 12 |
| 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 | 12 |
|---|---|
| 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. Viking Lab Oy was not found in either the U.S. or the Canadian register.