VH Pharma a.s.
CZ-MF-000005951 · Czechia · Praha
VH Pharma a.s. is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 6 |
|---|---|
| Class IIa | 2 |
Devices declared under this manufacturer
- HemaGel® NEW
- HemaGel® PROCTO
- HemaGel® SPRAY
Catalogue references include HN-100, HN-30, HN-5, HP-10, HP-15, HP-5.
European nomenclature codes declared: M04040501, M040499, M04040701.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| 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 | 8 |
|---|---|
| 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. VH Pharma a.s. was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
26 0172 QR/NB | issued | 2031-06-29 |
25 0399 QR/NB | issued | 2030-10-30 |
25 0237 QR/NB | issued | 2030-06-25 |