GeneProof a.s.
CZ-MF-000002370 · Czechia · Brno
GeneProof a.s. is registered in the European database on medical devices as a manufacturer, with 211 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- GeneProof Adenovirus MC PCR Kit
- GeneProof Aspergillus MC PCR Kit
- GeneProof CT/NG/MG Multiplex PCR Kit
- GeneProof Cytomegalovirus (CMV) MC PCR Kit
- GeneProof Enterovirus PCR Kit
- GeneProof Factor II Prothrombin MC PCR Kit
- GeneProof Human Herpesvirus 8 (HHV-8) MC PCR Kit
- GeneProof Human Papillomavirus (HPV) Screening PCR Kit
- GeneProof SARS-CoV-2 Advanced PCR Kit
- GeneProof VRE PCR Kit
- TaqPath™ Menu | GeneProof™ CT/NG/MG Multiplex PCR Kit
- TaqPath™ Menu | GeneProof™ Cytomegalovirus (CMV) PCR Kit
Showing 12 of 211 declared devices.
Catalogue references include A58117, A58429, ADV/MC/041, ASP/MC/038, CMV/MC/041, EV/ISEX/100.
European nomenclature codes declared: W0106010116, W0105011699, W0105900101, W0105040524, W010501080302, W0105040403.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 211 |
| 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 | 211 |
|---|---|
| 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. GeneProof a.s. was not found in either the U.S. or the Canadian register.