Hisztopatológia Kft.
HU-MF-000014417 · Hungary · Pécs
Hisztopatológia Kft. 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
Devices declared under this manufacturer
- HISTOLS BBPS Háttér gátló oldat
- HISTOLS Citrát puffer
- HISTOLS Peroxidáz gátló oldat
- HISTOLS-DAB
- HISTOLS-M
- HISTOLS-MR
- HISTOLS-MR-T
- HISTOLS-R
- HISTOLS-Rezisztens AEC
Catalogue references include 30010, 30011.500, 30011.M500, 30011.R500, 30012, 30014.K.
European nomenclature codes declared: W01029003, W01030711.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 10 |
| Country of registration | Hungary |
⚠️ 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. Hisztopatológia Kft. was not found in either the U.S. or the Canadian register.