DM CEOSA
ES-MF-000000579 · Spain · Alcorcon
DM CEOSA is registered in the European database on medical devices as a manufacturer, with 1 226 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 1 226 |
|---|
Devices declared under this manufacturer
- Arco con postes soldados de acero inoxidable INF. .016x.025in. 26mm
- Arco con postes soldados de acero inoxidable INF. .017x.025in. 46mm
- Arco con postes soldados de acero inoxidable INF. .018x.025in. 36mm
- Arco con postes soldados de acero inoxidable SUP. .016x.025in. 58mm
- Arco facial Cervera C3
- Arco facial Standard C-Modeler III
- Bracket rejilla soldada HILGERS Hook 14 .018in.
- Bracket rejilla soldada ROTH MINI 21 .018in.
- C-Modeler clase I BIMAXILAR E
- Equi-C POSTERIOR Nº36 Dcha.
- Mentonera 2 GANCHOS FORRADA Azul
- Plancha CUADRADA 120mm-1,5mm 15uds.
Showing 12 of 1 226 declared devices.
Catalogue references include 1131-AIL46, 1417-21, 1523-42, 2241-11, 2253-02, 2271-06.
European nomenclature codes declared: Q010403, Q010499, Q010405, Q010406.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 1 226 |
| 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 | 1 226 |
|---|---|
| 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. DM CEOSA was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
2024 PR 0037 | issued | 2029-09-16 |