Reha-Bed Sp. z o.o.
PL-MF-000040289 · Poland · Czeladź
Reha-Bed Sp. z o.o. is registered in the European database on medical devices as a manufacturer, with 314 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 314 |
|---|
Most frequent device types declared: B2/LOW/LUX/1200x2000, LEO.
Among these devices, 49 are declared active.
Devices declared under this manufacturer
- ASTER RECLINER ELECTRIC VIENNA 15 PLATINUM
- ASTER RECLINER MANUAL CADET ZEST 127 LILAC
- BARIATRIC 2
- ControlCare 1 78x187x15
- ControlCare 1 85x190x15\t
- ControlCare 1 87x200x10\t
- ControlCare 2 78x190x8
- ControlCare 3 90x200x14
- ControlCare 4 110x200x15
- LUNA
- MEDORA 3 Plus
- SZAFKA VIRGO CIEMNY ORZECH
Showing 12 of 314 declared devices.
Catalogue references include FTL/A2/02, M3ST8520S0M011600T00T13C21, MAT/CC1/78x187x15/REH/S, MAT/CC1/85x190x15/REH/S, MAT/CC1/87x200x10/REH/S, MAT/CC2/78x190x8/REH/S.
European nomenclature codes declared: V080702, V0499, V080202, V08060101, V08020101, V0805030102.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | REHA-BED SP. Z O.O. (PL) · FDA 3038613081 |
| Devices in EUDAMED | 314 |
| Country of registration | Poland |
Device-level evidence
| Devices with a numeric GTIN | 314 |
|---|---|
| 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: United States only. Reha-Bed Sp. z o.o. is registered in the United States but was not found in the Canadian register.