Anton Meyer & Co. AG
CH-MF-000040740 · Switzerland · Port
Anton Meyer & Co. AG is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 9 |
|---|
Most frequent device types declared: A-525, A-527, ME300, ME420MA, ME425.
Among these devices, 9 are declared reusable, 6 with a measuring function.
Authorised representative in the Union: MDSS GmbH.
Devices declared under this manufacturer
- Diamond Knife
Catalogue references include A-511, A-513, A-525, A-527, ME300, ME420MA.
European nomenclature codes declared: Q02010101.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | ANTON MEYER & CO. AG (CH) · FDA 8031019 |
| Devices in EUDAMED | 9 |
| Country of registration | Switzerland |
Device-level evidence
| Devices with a numeric GTIN | 9 |
|---|---|
| Found in the U.S. device database | 4 |
| Share | 44.4 % |
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: United States only. Anton Meyer & Co. AG is registered in the United States but was not found in the Canadian register.