Vevia Finland Oy
FI-MF-000006502 · Finland · Laitila
Vevia Finland Oy is registered in the European database on medical devices as a manufacturer, with 59 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 59 |
|---|
Devices declared under this manufacturer
- FlexCare 8906-75 200*75*13cm
- FlexCare 8906-85 200*85*13cm
- FlexCare Rescue 8907-75 200*75*13cm
- FlexCare Rescue 8907E Erikoismitta
- HighCare 8908-78 205*78*13cm
- HighCare 8908-85 200*85*13cm
- MEDIPLUS-hygieniapatja 90*200; MEPLUS90200
- Medi-hygieniapatja 90*200cm; ME90200
- Vevia Elasto Tripla RESC, RET230180, 200*80*13cm
- Vevia Tolkku, TOH230180, 200*80*13cm
- Vevia Tripla Max Rescue 200*80*17cm; TRIMAX RESC80200
- Vevia Vankka RESC, VA210190, 200*90*13cm
Showing 12 of 59 declared devices.
Catalogue references include FlexCare, FlexCare Rescue, Medi-patja, Vevia Elasto Tripla RESC, Vevia Tolkku, Vevia Vankka RESC.
European nomenclature codes declared: V080702.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 59 |
| 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 | 59 |
|---|---|
| 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. Vevia Finland Oy was not found in either the U.S. or the Canadian register.