PathoFinder B.V.
NL-MF-000002704 · Netherlands · Maastricht
PathoFinder B.V. is registered in the European database on medical devices as a manufacturer, with 10 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: PF0920-R, PF0966-R, PF0970-R, PF0971C-R, PF1200-2S.
Devices declared under this manufacturer
- 2SMARTFinder Color Compensation
- GastroFinder® 2SMART
- MeningoFinder® 2SMART
- RealAccurate® Quadruplex Atypical Bacteria PCR kit
- RealAccurate® Quadruplex Color Compensation v5
- RealAccurate® Quadruplex Influenza PCR Kit
- RealAccurate® Quadruplex Mycobacteria PCR kit
- RealAccurate® Quadruplex SARS-CoV-2 PCR Kit
- RespiFinder® 2SMART
- STD-Finder® 2SMART
Catalogue references include PF0920-R, PF0966-R, PF0970-R, PF0971C-R, PF1200-2S, PF2600-2S.
European nomenclature codes declared: W0101050199, W0105040519, W0105010703, W0104080207,W0105010117,W0105010305,W0105010803,W0105040311,W0105070501, W0105011099,W0105011499,W0105011606,W0105011899,W0105040501,W0105040506,W0105040516,W0105040530,W0105050201,W0105050208, W0105011103,W0105011105,W0105011305,W0105011503,W0105011610,W0105011611,W0105040205,W0105040311,W0105040403,W0105040502,W0105040521,W0105040524,W0105040704,W0105040804,W0105040904,W0105060403.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 10 |
| Country of registration | Netherlands |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 10 |
|---|---|
| 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. PathoFinder B.V. was not found in either the U.S. or the Canadian register.