MICROVAL
FR-MF-000003450 · France · Saint-Just-Malmont
MICROVAL is registered in the European database on medical devices as a manufacturer, with 161 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 161 |
|---|
Among these devices, 161 are declared sterile, 161 implantable.
Devices declared under this manufacturer
- 2D MESH
- 2F BUMP MESH L I
- 2F BUMP-MESH
- 2F MESH ANATOMIQUE
- 2F MESH Lichtenstein PET3D
- 2F MESH-3
- JG
- JP
- LF
- LG
- LT
- PS
Showing 12 of 161 declared devices.
Catalogue references include 411050, 413611/05, 413711, 413715, 414105, DS412060.
European nomenclature codes declared: P900202, P900205, H0102020199,H020201010102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 161 |
| 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 | 161 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | MICROVAL |
North American profile: Canada only. MICROVAL holds a Canadian licence but was not found in the U.S. register.