VIAMAR INTERNATIONAL, s.r.o.
CZ-MF-000038013 · Czechia · Praha
VIAMAR INTERNATIONAL, s.r.o. is registered in the European database on medical devices as a manufacturer, with 164 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- B.E.A. (Bile Esculin Azide) Agar
- BHI broth 5ml
- Buffered saline solution
- Buffered saline solution 1 ml
- Campylobacter selective agar (Karmali)
- Gardnerella vaginalis agar
- Lugol solution 1000ml (Gram)
- MacConkey agar / Deoxycholate-citrate agar
- Oxacillin agar 128u (ESBL)
- PureChrom UTI
- Sabouraud broth
- Sabouraud chloramphenicol gentamicin agar
Showing 12 of 164 declared devices.
Catalogue references include 98013-20, 98018-200, 98028-20, 98035-1, 98101-10, 98230-2.
European nomenclature codes declared: W0104010206, W0104010405, W0104030201, W0104010306, W0104030301, W0104010403.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 164 |
| 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 | 164 |
|---|---|
| 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. VIAMAR INTERNATIONAL, s.r.o. was not found in either the U.S. or the Canadian register.