Sendal, S.L.
ES-MF-000016981 · Spain · Almaraz
Sendal, S.L. is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 5 |
|---|
Most frequent device types declared: VH-33.
Among these devices, 5 are declared sterile.
Devices declared under this manufacturer
- BD Blood Transfusion Set
Catalogue references include VH-22-E3VGA, VH-26-EY3VGA, VH-27-EA, VH-33, VH-97-ERA.
European nomenclature codes declared: B010201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| 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 | 5 |
|---|---|
| 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. Sendal, S.L. was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
G15 064670 0029 | amended | 2027-10-23 |