MINEL Elektronikai és Kereskedelmi Korlátolt Felelősségű Társaság
HU-MF-000008069 · Hungary · Budapest
MINEL Elektronikai és Kereskedelmi Korlátolt Felelősségű Társaság is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 5 |
|---|
Among these devices, 2 are declared active.
Devices declared under this manufacturer
- 2 vezetékes páciens kábel TENSEL ME 2001-hez
- Köztianyagzsák TENS elektródákhoz
- Páciens kábel TENSEL DOUBLE SMART ME 2015-höz
- TENSEL DOUBLE SMART ME 2015
- TENSEL ME 2001
Catalogue references include ELSO-80-60, TDSPC-1.5-2, TENSEL DOUBLE SMART ME 2015, TENSEL ME 2001, TPC-1.5-2.
European nomenclature codes declared: Z120601, N010299,U070299,Z120604,Z120621,Z120622,Z12062701,Z12062801,Z12101106, N010201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| 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 | 5 |
|---|---|
| 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. MINEL Elektronikai és Kereskedelmi Korlátolt Felelősségű Társaság was not found in either the U.S. or the Canadian register.