ALFA VITA, s.r.o.
CZ-MF-000051941 · Czechia · Praha 5
ALFA VITA, s.r.o. is registered in the European database on medical devices as a manufacturer, with 74 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 74 |
|---|
Devices declared under this manufacturer
- FIXAplast CLASSIC 1m x 8cm
- FIXAplast CLASSIC 1m x 8cm COOP
- FIXAplast FIRST AID AQUA 24ks
- FIXAplast FIRST AID FAMILY MIX
- FIXAplast dětská strip 20ks COOP
- FIXAtape Classic 2,5cm x 5m
- FIXAtape STRETCH 10cm x 450cm tělová
- FIXAtape STRETCH 5 x 450cm, fluorescent green
- FIXAtape STRETCH 7,5 x 450cm, purple+black hearts
- FIXAtape STRETCH 7.5cm x 450cm modrá
- Obinadlo škrtící pryžové ESCHMARCH 60 x 1250mm
- VIX KIDS 0,5m x 6cm
Showing 12 of 74 declared devices.
Catalogue references include 0654, 0692, 1056, 11054, 11056, 1154.
European nomenclature codes declared: M030402020101, M050199, M050201, M0599, M050101, M050102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 74 |
| 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 | 74 |
|---|---|
| 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. ALFA VITA, s.r.o. was not found in either the U.S. or the Canadian register.