AVEFLOR, a.s.
CZ-MF-000003103 · Czechia · Kopidlno
AVEFLOR, a.s. is registered in the European database on medical devices as a manufacturer, with 32 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 32 |
|---|
Devices declared under this manufacturer
- AKUTOL™ Burn Spray
- AKUTOL™ STOP spray
- AKUTOL™ Sprej na popáleniny
- AKUTOL™ odstraňovač náplastí sprej
- AKUTOL™ spray
- AKUTOL™ sprej
- Akutol™ Plaster Remover Spray
- BLOOD STOP Spray
- Hemoflam®
- MULTINORM KӒLTE-SPRAY
- RYM® Protect
- Sensomed® Kälte-Spray
Showing 12 of 32 declared devices.
Catalogue references include SZ850013, Z070046, Z28, Z290000, Z300007, Z350000.
European nomenclature codes declared: M040599, M040499, M9001, M9003, Z12119005.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 32 |
| 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 | 32 |
|---|---|
| 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. AVEFLOR, a.s. was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
25 0380 QR/NB | supplemented | 2030-09-25 |