TEQUIR S.L.
ES-MF-000000783 · Spain · RIBARROJA DEL TURIA (VALENCIA)
TEQUIR S.L. is registered in the European database on medical devices as a manufacturer, with 71 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 39 |
|---|---|
| Class IIb | 32 |
Most frequent device types declared: Diameter Guide ø13, Diameter Guide ø17, Dynamometric Hudson T handle, Femoral Stem 120x13, Femoral Stem 140x18.
Among these devices, 32 are declared sterile, 32 implantable, 39 reusable.
Devices declared under this manufacturer
- Keep Walking Femoral Implant
- Keep Walking Reusable Surgical Devices
Showing 12 of 71 declared devices.
Catalogue references include TGUI0015680HU, TGUI0020213, TGUI0030114, TGUI0030300, TGUI0060000, TGUI3111213.
European nomenclature codes declared: P0999, L0916, L0922, L091102, L80, L99.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 71 |
| 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 | 71 |
|---|---|
| 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. TEQUIR S.L. was not found in either the U.S. or the Canadian register.