LABORATORIOS IBERPOS S.A.
ES-MF-000003372 · Spain · VIGO
LABORATORIOS IBERPOS S.A. is registered in the European database on medical devices as a manufacturer, with 102 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 102 |
|---|
Devices declared under this manufacturer
- CRUZ Y REIS Pensos plásticos Children 10 uds. 1 tam.
- CRUZ Y REIS Pensos sensitive 20 Uds. 3 tam.
- DR. LINE Apósitos Invisibles 20 Uds. 4 tam.
- DR. LINE Esparadrapo Textil 5 m. x 2,5 cm. 1 Ud.
- HERBIPLAST NEW apósitos infantiles 10 Uds. 1 tam.
- HERBIPLAST NEW apósitos tela 10 Uds. 1 tam.
- PLUSKIT Plastic pack mediano 20 Uds. 2 tam.
- SOFARMA Penso Cínico resistente à água 10 x15 cm. 4 uds.
- SOFARMA Pensos Clínicos 7,5 x 5 cm. 5 Uds.
- TIRAPLASTIC Plastic azul detectable pack XL 100 Uds. 1 tam.
- TIRAPLASTIC Plastic azul detectable pack mediano 20 Uds. 1 tam.
- TIRAPLASTIC Plastic pack grande 30 Uds. 4 tam.
Showing 12 of 102 declared devices.
Catalogue references include 20-APO000060, 23-BOT000030, 71-CYR000020, 71-CYR000030, 71-DRL000320, 71-HER010125.
European nomenclature codes declared: M04010102, M04010199, M04010101, M050101.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | LABORATORIOS ZEPOL S.A. (CR) · FDA 3004637474 |
| Devices in EUDAMED | 102 |
| Country of registration | Spain |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 102 |
|---|---|
| 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.