VITRO, S.A.
ES-MF-000001498 · Spain · Sevilla
VITRO, S.A. is registered in the European database on medical devices as a manufacturer, with 111 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
Most frequent device types declared: MAD-001560Q, MAD-003955M-EX-A8, MAD-004077R1, MAD-004080VS, MAD-103.008.
Devices declared under this manufacturer
- Master Diagnóstica
- master diagnostica
- master diagnóstica
Showing 12 of 111 declared devices.
Catalogue references include MAD-001560Q, MAD-003955M-EX-A8, MAD-004080VS, MAD-103.008, MAD-FISH-PK, MAD-FISH-PTK.
European nomenclature codes declared: W01030799, W01030711, W01030708, W02079099, W05019099, W01019002.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | VITRO S.A. (ES) · FDA 3014611360 |
| Devices in EUDAMED | 111 |
| Country of registration | Spain |
Device-level evidence
| Devices with a numeric GTIN | 111 |
|---|---|
| Found in the U.S. device database | 27 |
| Share | 24.3 % |
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. VITRO, S.A. is registered in the United States but was not found in the Canadian register.