CASCINATION AG
CH-MF-000009927 · Switzerland · Bern
CASCINATION AG is registered in the European database on medical devices as a manufacturer, with 17 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 13 |
|---|---|
| Class IIb | 4 |
Among these devices, 10 are declared active, 8 with a measuring function.
Authorised representative in the Union: CAScination Deutschland GmbH.
Devices declared under this manufacturer
- CAS-One IR Accessory Tray A
- CAS-One IR Aiming Device A
- CAS-One IR Baseplate A
- CAS-One IR Cushion A
- CAS-One IR Guide Arm A
- CAS-One IR Marker Template
- CAS-One IR Platform A
- CAS-One IR Pointer A
- CAS-One IR Software
- OTODRIVE
- OTOPLAN
Showing 12 of 17 declared devices.
Catalogue references include 10006, 20072, 30007, 30026, 30085, 30238.
European nomenclature codes declared: Z12011480, Z12140592, Z12011492, Z12011485, Q030499.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | CASCINATION (CH) · FDA 3011797532 |
| Devices in EUDAMED | 17 |
| Country of registration | Switzerland |
Device-level evidence
| Devices with a numeric GTIN | 17 |
|---|---|
| Found in the U.S. device database | 1 |
| Share | 5.9 % |
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. CASCINATION AG is registered in the United States but was not found in the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
G10 095657 0006 | issued | 2027-05-29 |