PROMA REHA, s.r.o.
CZ-MF-000013860 · Czechia · Česká Skalice
PROMA REHA, s.r.o. is registered in the European database on medical devices as a manufacturer, with 59 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 59 |
|---|
Among these devices, 47 are declared active, 12 with a measuring function.
Devices declared under this manufacturer
- DOMEO E
- DOMEO H
- DOMEO M
- ELEVA H
- Hrazda s hrazdičkou
- INVENT
- PRESTO
- SPARO
- SUPERTA H
- SUPERTA M
- U-2B
- URGENT TOP
Showing 12 of 59 declared devices.
Catalogue references include DOMEO-M-85, DOMEO-M-90, INVENT-2C, PRESTO, SPARO, SUPERTA-M-80.
European nomenclature codes declared: V08060101, V080602, V080702, V08050101, V080603, Y120606.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 59 |
| Country of registration | Czechia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 59 |
|---|---|
| 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. PROMA REHA, s.r.o. was not found in either the U.S. or the Canadian register.