LABORATORIOS HARTMANN S.A.
ES-MF-000002991 · Spain · Mataró
LABORATORIOS HARTMANN S.A. is registered in the European database on medical devices as a manufacturer, with 19 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 19 |
|---|
Most frequent device types declared: Esparadrapo papel, Omnipor, Esparadrapo tela.
Devices declared under this manufacturer
- Esparadrapo papel
- Esparadrapo tela
- Omniplast Blanco
- Omniplast carne
- Omnipor
- Omnipor skin color
Showing 12 of 19 declared devices.
Catalogue references include 9005942, 9006842, 9006861, 9006912, 9006932, 9006940.
European nomenclature codes declared: M050199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 19 |
| 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 | 19 |
|---|---|
| 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. LABORATORIOS HARTMANN S.A. was not found in either the U.S. or the Canadian register.