EGO Zlín, spol. s r.o.
CZ-MF-000031911 · Czechia · Zlín
EGO Zlín, spol. s r.o. is registered in the European database on medical devices as a manufacturer, with 28 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 28 |
|---|
Most frequent device types declared: AME-FP, EBCT, EM, EPV, ES-13.
Devices declared under this manufacturer
- Aktivní antidekubitní matrace
- Biobox EBXT na tubusové konstrukci
- Dětský zádržný systém redukovaný, bez vakuové vložky
- EBV-AERO
- EBV-NEO
- Perinatologický vak základní
- Vakuová dlaha na dlaha na dolní končetinu klasická
- Vakuová dlaha na dolní končetinu s opěrkou chodidla, dětská
- Vakuová dlaha na horní končetinu dětská
- Vakuová dlaha na horní končetinu klasická
- Vakuová dlaha na horní končetinu pravoúhlá
- Vakuová matrace jednokomorová v textilním obalu
Showing 12 of 28 declared devices.
Catalogue references include EBV-NEO, EM-10/7 RL, EPV-10, ES-10, ES-10/P, ES-11.
European nomenclature codes declared: T030599, V08050103, M03050202, V08050199, V080701, M03050299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 28 |
| 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 | 28 |
|---|---|
| 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. EGO Zlín, spol. s r.o. was not found in either the U.S. or the Canadian register.