FRANKLAB
FR-MF-000013243 · France · Le Perray-En-Yvelines
FRANKLAB is registered in the European database on medical devices as a manufacturer, with 102 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 74 |
|---|---|
| Class IIb | 28 |
Devices declared under this manufacturer
- AT CLEAR NEUTRA
- BACTI FINAL - 5L
- BACTI FIRST - 5L
- CA 22 - 5L low can
- CA 5P
- ECOSEPTOL FOAM - 5L
- ENZYMEX LD - 5L Gerbable opercule thermoscellé
- Enzymex L4
- Enzymex P - 2Kg
- NEUTRAX PF
- PHOSPHAX - 10L
- TFD 14 -1000L
Showing 12 of 102 declared devices.
Catalogue references include 1012401, 1020889, 1026695, 1032005, 1032011AT, 1044905GPO.
European nomenclature codes declared: D0899, V0799, D99, D0801, D050103, D0799.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 102 |
| 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 | 102 |
|---|---|
| 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. FRANKLAB was not found in either the U.S. or the Canadian register.