RUHER IBERICA, S.A.
ES-MF-000055875 · Spain · Montcada i Reixac
RUHER IBERICA, S.A. is registered in the European database on medical devices as a manufacturer, with 20 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 20 |
|---|
Most frequent device types declared: Gasas de algodón, PE Skin Color perforated 7x2 cm.
Devices declared under this manufacturer
- Apósitos Baikim classic 10U
- Apósitos Baikim classic surtidos 50 U
- Apósitos codo-rodilla Baikim sport
- Baikim BIO apósitos 10 unds
- Baikim apósitos baby 16U
- Baikim classic apósitos 20 U
- Baikim classic apósitos para cortar
- Baikim soft apósitos 15 U
- Baikim soft apósitos para dedos
- Baikim soft apósitos para rozaduras
- Baikim soft maxi apósito 7.5 x 5 cm
- Baikim sport apósitos nasales
Showing 12 of 20 declared devices.
Catalogue references include 45802, 45803, 45804, 45805, 45811, 45816.
European nomenclature codes declared: M04010102, M04010101, M04010199, M0201010102, M040701, M0303010101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 20 |
| 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 | 20 |
|---|---|
| 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. RUHER IBERICA, S.A. was not found in either the U.S. or the Canadian register.