Espeon, s.r.o.
CZ-MF-000049569 · Czechia · Praha 8
Espeon, s.r.o. is registered in the European database on medical devices as a manufacturer, with 178 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 178 |
|---|
Devices declared under this manufacturer
- LATEX BLACK
- LATEX BLUE
- LATEX FIT
- NITRIL CARE
- NITRIL COMFORT
- NITRIL DIAMOND
- NITRIL IDEAL
- NITRIL LONG
- NITRIL PREMIUM
- NITRIL PREMIUM3
- NITRIL SOFT
- NITRIL SPARKLE
Showing 12 of 178 declared devices.
Catalogue references include 100005, 100052, 100106, 100125, 100174, 100175.
European nomenclature codes declared: T01020204, T01020201, T010201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 178 |
| 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 | 178 |
|---|---|
| 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. Espeon, s.r.o. was not found in either the U.S. or the Canadian register.