BIOCORP PRODUCTION
FR-MF-000011122 · France · ISSOIRE
BIOCORP PRODUCTION is registered in the European database on medical devices as a manufacturer, with 24 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 24 |
|---|
Most frequent device types declared: Connected-MD, Connected-SWMD, Measuring-MD.
Among these devices, 5 are declared with a measuring function.
Devices declared under this manufacturer
- APPLICATEUR 1G GYDRELLE
- COMPTE-GOUTTES OPV
- CONNECTDROP APP
- FLEXPRO FR/DE
- MALLYA D CZE
- MALLYA G SVN
- MALLYA OZEM - EU1
- PIPETTE DOSEUSE 1-25KG
- PIPETTE DOSEUSE 5-25KG
- SOLOSMART AT/DE/NL/SE
- SOLOSMART CA
- SOLOSMART CZ/GR/PL
Showing 12 of 24 declared devices.
Catalogue references include 0113264, 0113472, 0113657, 0173980 2.0.X IOs, 0174221, 0174313.
European nomenclature codes declared: Z12040199, A0704, Z12040192.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 24 |
| 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 | 24 |
|---|---|
| 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. BIOCORP PRODUCTION was not found in either the U.S. or the Canadian register.