BCB Medical Oy
FI-MF-000002441 · Finland · TURKU
BCB Medical Oy is registered in the European database on medical devices as a manufacturer, with 82 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 82 |
|---|
Devices declared under this manufacturer
- BCB 15D Register
- BCB Cataract Register
- BCB Child & adolesc. psychiatry Register
- BCB Cleft lip and palate Register
- BCB Diabetes Register
- BCB General psychiatry Register
- BCB Hip Register
- BCB Kids' spine Register
- BCB Lymphoma Register
- BCB Myeloma Register
- BCB Neonatal intensive care Register
- BCB Out-of-hospital cardiac arrest Register
Showing 12 of 82 declared devices.
Catalogue references include 06430078510042, 06430078510516, 06430078510523, 06430078510547, 06430078510691, 06430078510806.
European nomenclature codes declared: V92.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 82 |
| 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 | 82 |
|---|---|
| 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. BCB Medical Oy was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
FI23/0000002 | supplemented | 2027-01-22 |
FI23/0000002 | reissued | 2031-02-11 |