TODA PHARMA
FR-MF-000007152 · France · Strasbourg
TODA PHARMA is registered in the European database on medical devices as a manufacturer, with 27 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: Toda Dengdiag combo 1, Toda Malariadiag V2, Toda Multidiag 11, Toda Multidiag 8, Toda Preterm Diag.
Devices declared under this manufacturer
- Toda Coronadiag Ag
- Toda Dengdiag combo 1
- Toda Infludiag A&B
- Toda Malariadiag V2
- Toda Multidiag 11
- Toda Multidiag 8 - Box of 50
- Toda Preterm Diag
- Toda Preterm Diag 20
- Toda Strepdiag A
- Toda Strepdiag B 1
- Toda Tetanusdiag 10
- Toda XPER DIAG
Showing 12 of 27 declared devices.
Catalogue references include 1008-50, 1011-100, 1029, 1062, 21GO1-20, 2271-10.
European nomenclature codes declared: W0102050299, W0101060204, W0105040619, W0105040611, W0102160302, W0105011104.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 27 |
| 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 | 27 |
|---|---|
| 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. TODA PHARMA was not found in either the U.S. or the Canadian register.