CHIROMEGA
SK-MF-000024150 · Slovakia · Humenné
CHIROMEGA is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 6 |
|---|
Most frequent device types declared: CHIROMEGA 654, CHIROMEGA 654 CART, CHIROMEGA 654 DUET, CHIROMEGA 654 NK, CHIROMEGA 654 Nika.
Among these devices, 6 are declared active.
Devices declared under this manufacturer
- CHIROMEGA s.r.o.
Catalogue references include CHIROMEGA 654, CHIROMEGA 654 CART, CHIROMEGA 654 DUET, CHIROMEGA 654 NIKA, CHIROMEGA 654 NK, CHIROMEGA 654 SOLO.
European nomenclature codes declared: Z12110101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| Country of registration | Slovakia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 6 |
|---|---|
| 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. CHIROMEGA was not found in either the U.S. or the Canadian register.