Telic, S.A.U.
ES-MF-000001853 · Spain · Bigues i Riells
Telic, S.A.U. is registered in the European database on medical devices as a manufacturer, with 299 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIb | 97 |
|---|---|
| Class IIa | 202 |
Most frequent device types declared: 2125-C/00, EDC-1020, EDC-1050, EDC-1055, EDC-1090.
Among these devices, 7 are declared sterile, 7 reusable, 189 active.
Devices declared under this manufacturer
- ADNPRO
- Blayco
- COMEPA
- DESFI-DORMO
- DORMO
- DORMO-SPEC
- Dormo-Strip
- HOSPITAL'S PLATE
- MEDIKAS
- MIPMED
- OXD PROFESSIONALCARE
- TENSI+
Showing 12 of 299 declared devices.
Catalogue references include 0350/R, 2225, 2500-C12, 4212, EDC-2035, EDC-2045.
European nomenclature codes declared: K02010202, C020480, Z11040185, C020501, Z12021085, V9099.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | TELIC, S.A.U. (ES) · FDA 3012693071 |
| Devices in EUDAMED | 299 |
| Country of registration | Spain |
Device-level evidence
| Devices with a numeric GTIN | 299 |
|---|---|
| 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: United States only. Telic, S.A.U. is registered in the United States but was not found in the Canadian register.