Abílio Freire Lda
PT-MF-000022553 · Portugal · Freamunde
Abílio Freire Lda is registered in the European database on medical devices as a manufacturer, with 85 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 85 |
|---|
Devices declared under this manufacturer
- AFRE
- DIMOR
Showing 12 of 85 declared devices.
Catalogue references include 01020415W, DM1030510B, DM1050307B, DM1061007B, DM1070520B, DM1120315B.
European nomenclature codes declared: M030101, M0303010101, M030402010101, M03050299, M03040199, M03030202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 85 |
| Country of registration | Portugal |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 85 |
|---|---|
| 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. Abílio Freire Lda was not found in either the U.S. or the Canadian register.