MEDIDERMA S.L.
ES-MF-000001648 · Spain · Puzol
MEDIDERMA S.L. is registered in the European database on medical devices as a manufacturer, with 15 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 15 |
|---|
Among these devices, 14 are declared sterile, 1 active.
Devices declared under this manufacturer
- Nanopore Stylus
Showing 12 of 15 declared devices.
Catalogue references include 40002734, 40003042, 40003394, 40004233, 40004234, 40004235.
European nomenclature codes declared: A019099, Z12040203.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 15 |
| 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 | 15 |
|---|---|
| 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. MEDIDERMA S.L. was not found in either the U.S. or the Canadian register.