Scanatron AG
CH-MF-000013600 · Switzerland · Affoltern am Albis
Scanatron AG is registered in the European database on medical devices as a manufacturer, with 41 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 41 |
|---|
Most frequent device types declared: SOL20-3-V, SEL21, Sterilhandgriff, SUL22.
Among these devices, 4 are declared reusable, 37 active.
Authorised representative in the Union: NL-AR-000013145.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 41 |
| Country of registration | Switzerland |
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.