LIDERMED S.A.
ES-MF-000004664 · Spain · MATARO
LIDERMED S.A. is registered in the European database on medical devices as a manufacturer, with 163 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 163 |
|---|
Most frequent device types declared: APÓSITOS PARA HERIDAS, LLAGAS Y ÚLCERAS, COLLARIN CERVICAL BLANDO, COLLARIN CERVICAL CONTINUO, INMOVILIZADOR DE CLAVICULA, SOPORTE CABESTRILLO.
Among these devices, 10 are declared sterile.
Devices declared under this manufacturer
- ALIVIODERM
- ALIVIOVISCO
- ARMEX ROLL
- ARMEX STANDARD
- COLLARIN CERVICAL BLANDO
- LIDERFIX
- LIDERFIX 1 m.
- LIDERGRIP
- LIDERGRIP 1m.
- LIDERGRIP 20/1
- LIDERGRIP EMBO
- LIDERTON
Showing 12 of 163 declared devices.
Catalogue references include 0011104, 0020401, 0021201, 0021206, 0030407, 0030801.
European nomenclature codes declared: M030499, M03030103, M040499, M0303010101, Y060312, M030405.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 163 |
| 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 | 163 |
|---|---|
| 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. LIDERMED S.A. was not found in either the U.S. or the Canadian register.