RAMED Kopřivnice s.r.o.
CZ-MF-000043587 · Czechia · Kopřivnice
RAMED Kopřivnice s.r.o. is registered in the European database on medical devices as a manufacturer, with 33 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 33 |
|---|
Most frequent device types declared: PPZ, SOSVD, UOS.
Among these devices, 31 are declared active.
Devices declared under this manufacturer
- Endoskopicko-rentgenologický stůl s plovoucí deskou RAMED
- Překládací zařízení pro operační sály PPZ 01
- Systém operačních stolů s výměnnou pracovní deskou RAMED
- Universální operační stůl RAMED
Showing 12 of 33 declared devices.
Catalogue references include 2520-07, 4300 VD-00, 4300-03, 5200-00, 5300-07, 6300 VD-09.
European nomenclature codes declared: Z12011202, Z12019010.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 33 |
| 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 | 33 |
|---|---|
| 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. RAMED Kopřivnice s.r.o. was not found in either the U.S. or the Canadian register.