Reiner Medtech S.L.U
ES-MF-000048477 · Spain · Itziar - Deba
Reiner Medtech S.L.U is registered in the European database on medical devices as a manufacturer, with 16 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 16 |
|---|
Most frequent device types declared: DISPOSITIVO PARA INCONTINENCIA URINARIA MASCULINA URICLAK, Dosivent, MASCARILLA SILICONA.
Devices declared under this manufacturer
- Dosivent
- URICLAK
Showing 12 of 16 declared devices.
Catalogue references include 00540EAM010, 00540EAM040, 00540EAZ010, 00540ENA010, 00540ENA040, 00600INT000.
European nomenclature codes declared: Z12159002, R03010301, T0499.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 16 |
| 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 | 16 |
|---|---|
| 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. Reiner Medtech S.L.U was not found in either the U.S. or the Canadian register.