FARMABAN s.a.
ES-MF-000004713 · Spain · Sant Fruitós de Bages
FARMABAN s.a. is registered in the European database on medical devices as a manufacturer, with 298 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 298 |
|---|
Most frequent device types declared: CPK SHOULDER ROLL.
Devices declared under this manufacturer
- Absoplast
- CPK FORM
- CPK SPORT
- ElastiPHAR
- Extensa PLUS
- Klinidur ® cohesive bandage
- LENO K TAPE
- LENOPLAST
- LENOPLAST Sport
- LENOSOFT
- LENOTAPE
- MasterKompress 2 Lite
Showing 12 of 298 declared devices.
Catalogue references include 1144, 1284.1, 13229, 1350, 1514, 1628.
European nomenclature codes declared: M030499, M03030199,M030499, M0303010201, M03040199, M03030103, M03040299.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | FARMABAN S.A. (ES) · FDA 3003984013 |
| Devices in EUDAMED | 298 |
| Country of registration | Spain |
Device-level evidence
| Devices with a numeric GTIN | 298 |
|---|---|
| Found in the U.S. device database | 5 |
| Share | 1.7 % |
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. FARMABAN s.a. is registered in the United States but was not found in the Canadian register.