Seid
ES-MF-000004010 · Spain · Lliça de Vall (Barcelona)
Seid is registered in the European database on medical devices as a manufacturer, with 13 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 9 |
|---|---|
| Class IIa | 4 |
Devices declared under this manufacturer
- FURADERM
- FURADERM 100g
- FURADERM 30g
- SEIDIGYN 30 g
- SEIDIGYN 5g
- SEIDYCALM
- SEIDYLUBE
- SEIDYLUBE [ES]
- Seidigyn crema calmante íntima
- Seidigyn gel lubricante íntimo
Showing 12 of 13 declared devices.
Catalogue references include 193404.8, 193404.8M, 193405.5, 216445.1, 217318.7, 217318.7M.
European nomenclature codes declared: U0803, U0899, M9002.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 13 |
| Country of registration | Spain |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 13 |
|---|---|
| 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. Seid was not found in either the U.S. or the Canadian register.