ABANZA TECNOMED, S.L.
ES-MF-000007530 · Spain · Mutilva
ABANZA TECNOMED, S.L. is registered in the European database on medical devices as a manufacturer, with 25 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 21 |
|---|---|
| Class IIb | 4 |
Most frequent device types declared: 21.
Among these devices, 4 are declared sterile, 4 implantable, 21 reusable.
Devices declared under this manufacturer
- Countersink Tool
- Inserter Coupling Screw 7mm & 8mm
- Inserter Coupling Screw 9mm & 10mm
- Positioner Guide
- Sterilization tray 7mm - 10 mm
- WasherCap™ Countersink 8mm
- WasherCap™ Countersink Positioner 10mm
- WasherCap™ Countersink Positioner 9mm
- WasherCap™ Fixation System 7mm
- WasherCap™ Fixation System 8mm
- WasherCap™ Fixation System 9mm
- WasherCap™ Inserter 7mm & 8mm
Showing 12 of 25 declared devices.
Catalogue references include ABWC0721, ATMWCIN 42, ATMWCIN07, ATMWCIN40, ATMWCIN52, ATMWCIN78.
European nomenclature codes declared: L091102, P09120699, L098099, L091101, L091104, S010401.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | ABANZA TECNOMED, S.L. (ES) · FDA 3025608439 |
| Devices in EUDAMED | 25 |
| Country of registration | Spain |
Device-level evidence
| Devices with a numeric GTIN | 25 |
|---|---|
| Found in the U.S. device database | 24 |
| Share | 96.0 % |
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. ABANZA TECNOMED, S.L. is registered in the United States but was not found in the Canadian register.