VINAMET CZ s.r.o.
CZ-MF-000003732 · Czechia · Havířov
VINAMET CZ s.r.o. is registered in the European database on medical devices as a manufacturer, with 34 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 34 |
|---|
Most frequent device types declared: Miska 500 ml žlutá V-MA-002/Z.
Among these devices, 27 are declared with a measuring function.
Devices declared under this manufacturer
- Ledvinka 1500 ml modrá V-LE-002/M
- Ledvinka 1500 ml červená V-LE-002/C
- Ledvinka 800 ml V-LE-001
- Ledvinka 800 ml červená V-LE-001/C
- Miska 1000 ml V-MA-003
- Miska 1000 ml modrá V-MA-003/M
- Miska 250 ml V-MA-001
- Miska 250 ml modrá V-MA-001/M
- Miska 250 ml červená V-MA-001/C
- Miska 500 ml modrá V-MA-002/M
- Miska na skalpel V-MS-001
- Odměrka V-OD-001
Showing 12 of 34 declared devices.
Catalogue references include V-LE-001, V-LE-002/C, V-LE-002/M, V-MA-001/C, V-MA-002/M, V-MA-003.
European nomenclature codes declared: V0399, A99, A13.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 34 |
| 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 | 34 |
|---|---|
| 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. VINAMET CZ s.r.o. was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
24 0237 QR/NB | issued | 2029-06-25 |