LDBIO DIAGNOSTICS
FR-MF-000021697 · France · LYON
LDBIO DIAGNOSTICS is registered in the European database on medical devices as a manufacturer, with 47 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- ASPERGILLUS ICT IgG-IgM
- ASPERGILLUS WB IgG
- CHAGAS WB IgG
- CYSTICERCOSIS WB IgG
- ECHINOCOCCUS WB IgG
- LEISHMANIA WB IgG
- PEO ICT IgG-IgM
- PEO WB IgG
- SCHISTO II WB IgG
- SCHISTOSOMA ICT IgG-IgM
- TOXOCARA WB IgG
- TOXOPLASMA ICT IgG-IgM
Showing 12 of 47 declared devices.
Catalogue references include BILZ Ab ICT100, BILZ Ab ICT20, CHA-WB96G, MPEO Ab ICT100, TOXO Ab ICT100, TRI ES-WB12G.
European nomenclature codes declared: W0105050299, W0105050206, W01020299, W0105060301, W0105050202, W0105050205.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 47 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
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. LDBIO DIAGNOSTICS was not found in either the U.S. or the Canadian register.