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: SEL21, SOL20-3-V, SUL22, Sterilhandgriff.
Among these devices, 4 are declared reusable, 37 active.
Authorised representative in the Union: Scanatron International NL.
Devices declared under this manufacturer
- SEL21-3
- SEL21-3-L
- SEL21-4-L
- SEL21-4-V
- SEL21-4C
- SOL20-3
- SOL20-3-V
- SOL20-3C
- SOL20-4
- SOL20-4-H
- SOL20-5-V
- SOL20-5C
Showing 12 of 41 declared devices.
Catalogue references include 10.0000.02, 20.3300.000, 20.4110.000, 20.5125.000, 20.5305.000, 21.3100.000.
European nomenclature codes declared: Z12010701,Z12010702, Z12010780.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 41 |
| 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 | 41 |
|---|---|
| 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. Scanatron AG was not found in either the U.S. or the Canadian register.