MDB TEXINOV
FR-MF-000001728 · France · Saint Didier de la tour
MDB TEXINOV is registered in the European database on medical devices as a manufacturer, with 42 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 42 |
|---|
Most frequent device types declared: Source FluxmedicareV2.
Devices declared under this manufacturer
- Cap 1
- FLUXMED 1V1
- FLUXMED 3V1
- FLUXMED1-V2
- FLUXMED2-V2
- HARN2
- TEXTLIGHT2-V2
- TEXTLIGHT3-V2
- TEXTLIGHT4-V2
- TEXTLIGHT6-V2
- Texishield CH-B02
- Texishield CH-C01
Showing 12 of 42 declared devices.
Catalogue references include CH-B02, CH-C01, FLUXMED 1V1, FLUXMED 1V2, FLUXMED 2V2, HARN2 Harnais.
European nomenclature codes declared: Z12040280, T020603, T020604, Z12040285, Z12040202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 42 |
| 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 | 42 |
|---|---|
| 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. MDB TEXINOV was not found in either the U.S. or the Canadian register.