Evidencio
NL-MF-000008386 · Netherlands · Haaksbergen
Evidencio is registered in the European database on medical devices as a manufacturer, with 34 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 34 |
|---|
Among these devices, 34 are declared active.
Devices declared under this manufacturer
- ABC Bleeding Risk Score Calculator
- ABC Stroke Risk Score Calculator
- ADHERE Algorithm
- ADNEX model
- AHA GWTG-HF Risk Score
- ATRIA Bleeding Risk Score Calculator
- HAS-BLED Score
- HOSPITAL Score
- INFLUENCE 3.0
- MELD Na
- ORBIT Bleeding Risk Score Calculator
- SCORE2
Showing 12 of 34 declared devices.
Catalogue references include 10085, 162, 2187, 2238, 2326, 2496.
European nomenclature codes declared: V92, Z12059092.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 34 |
| Country of registration | Netherlands |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 34 |
|---|---|
| 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. Evidencio was not found in either the U.S. or the Canadian register.