medmix Switzerland AG
CH-MF-000016467 · Switzerland · Haag
medmix Switzerland AG is registered in the European database on medical devices as a manufacturer, with 145 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 145 |
|---|
Authorised representative in the Union: medmix Deutschland GmbH.
Devices declared under this manufacturer
- A Silicone 380 Dynamic Mixer
- CyberTech Mixing Tips
- Intra Oral Tip
- MIXPAC Vmix
- MIXPAC Vmix Mixing Tip
- Mixing Tips
- Mixing Tips YELLOW
- Root Canal Tip
- System 380 Mixing Tips
- T-Mixer
- T-Mixer Colibri Mixing Tip
- T-Mixer Colibri Plus Breakable
Showing 12 of 145 declared devices.
Catalogue references include 162974, 167145, 167615, 167619, 182322, 186103.
European nomenclature codes declared: Q010506, Q019006, Q0199.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | medmix Switzerland AG (CH) · FDA 3007497008 |
| Devices in EUDAMED | 145 |
| Country of registration | Switzerland |
Device-level evidence
| Devices with a numeric GTIN | 145 |
|---|---|
| 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: United States only. medmix Switzerland AG is registered in the United States but was not found in the Canadian register.