ELITECH MICROBIO
FR-MF-000025235 · France · Signes
ELITECH MICROBIO is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: 00061, 00064, 00083, 66604, 66610.
Devices declared under this manufacturer
- E.L.I.H.A TOXO
- ELI.H.A Echinococcus
- ELIStain Paratest
- HYDATIDOSE
- MYCOPLASMA Stabilizer
- TOXO HAI
- UMMt AMIES RevolutioN
- UMMt RevolutioN
Catalogue references include 00061, 00064, 00083, 5248, 5250, 66604.
European nomenclature codes declared: W0105050101, W0105050204, W0104010203, W0104050199, W0104010899.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 8 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | ELITECH MICROBIO |
North American profile: Canada only. ELITECH MICROBIO holds a Canadian licence but was not found in the U.S. register.