REAGENS Fejlesztő, Gyártó és Kereskedelmi Kft.
HU-MF-000019161 · Hungary · Budapest
REAGENS Fejlesztő, Gyártó és Kereskedelmi Kft. is registered in the European database on medical devices as a manufacturer, with 21 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: AGGI-LISS, AKTÍV LIOFILIZÁLT PAPAIN, Bromelin, Pufferolt fiziológiás sóoldat, Pufferolt fiziológiás sóoldat Plus.
Devices declared under this manufacturer
- AGGI-LISS
- Aktív liofilizált papain
- Bromelin 1000 ml
- Bromelin 30 ml
- Pufferolt fiziológiás sóoldat
- Pufferolt fiziológiás sóoldat 10000 ml
- Pufferolt fiziológiás sóoldat 3000 ml
- Pufferolt fiziológiás sóoldat 5000 ml
- Pufferolt fiziológiás sóoldat Plus 3000 ml
- REAG-BLUE Panoptic
- REAG-FIX Panoptic
- REAG-QUICK Panoptic
Showing 12 of 21 declared devices.
Catalogue references include 11114, 13103, 15015, 15018, 21217, 31010.
European nomenclature codes declared: W0103010399, W0101070304, W0103030307, B07, W0103030306.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 21 |
| 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 | 21 |
|---|---|
| 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. REAGENS Fejlesztő, Gyártó és Kereskedelmi Kft. was not found in either the U.S. or the Canadian register.