Surgify Medical Oy
FI-MF-000017137 · Finland · Espoo
Surgify Medical Oy is registered in the European database on medical devices as a manufacturer, with 23 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 23 |
|---|
Most frequent device types declared: 100-54-TL, 100-54-TM, Surgify Halo.
Among these devices, 23 are declared sterile.
Devices declared under this manufacturer
- Surgify Halo
- Surgify Safety Burr
Showing 12 of 23 declared devices.
Catalogue references include 100-54-SE, 100-54-TM, 30.070.NVG.H2, 30.125.NVG.H2, 40.000.SEE.H1, 40.070.NVG.H1.
European nomenclature codes declared: V901699, V0199,Z12100985,Z12130585,Z12149085.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | SURGIFY MEDICAL OY (FI) · FDA 3015392173 |
| Devices in EUDAMED | 23 |
| Country of registration | Finland |
Device-level evidence
| Devices with a numeric GTIN | 21 |
|---|---|
| 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: United States only. Surgify Medical Oy is registered in the United States but was not found in the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
CR-03-1203-838-24 | supplemented | 2029-03-15 |