Linde France
FR-MF-000000961 · France · Lyon Cedex 07
Linde France is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 4 |
|---|---|
| Class IIb | 4 |
Most frequent device types declared: B02, B05, B15.
Among these devices, 7 are declared active.
Devices declared under this manufacturer
- Argon médical chirurgical
- Protoxyde d'azote cryogénique médical
- Système de distribution de gaz médicaux
- VISIOSTAR 2
- VISIOSTAR 3
- VISIOSTAR 3.1
Catalogue references include 12040128, 3680102, 3680105, 3690134, NA, R613850.
European nomenclature codes declared: Z120309, V0904, V0905.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| 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 | 8 |
|---|---|
| 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. Linde France was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
HZ 2360710-1 | issued | 2029-12-22 |
DZ 2360710-1 | issued | 2029-12-22 |