Messer Schweiz AG
CH-MF-000042206 · Switzerland · Lenzburg
Messer Schweiz AG 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 | 7 |
|---|---|
| Class IIb | 1 |
Most frequent device types declared: 10L Cylinder, 10L Cylinder STR, 13L Cylinder, 2L Cylinder, 4L Cylinder.
Among these devices, 1 are declared reusable, 1 active, 1 with a measuring function.
Authorised representative in the Union: Axxos GmbH.
Catalogue references include 0776999002, 103020022, 103020042, 103020102, 10302052, 103026042.
European nomenclature codes declared: V0901, Z120309.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| Country of registration | Switzerland |
⚠️ 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. Messer Schweiz AG was not found in either the U.S. or the Canadian register.