Chemichl AG
LI-MF-000018069 · Liechtenstein · Vaduz
Chemichl AG is registered in the European database on medical devices as a manufacturer, with 431 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 431 |
|---|
Most frequent device types declared: Dentalkeramik.
Among these devices, 431 are declared implantable.
Devices declared under this manufacturer
- 850 MiYO FISSURE fluor.
- InSync MC DENTIN B0
- InSync MC MARGIN B1
- InSync MC Schneide 2
- InSync MODELLING LIQUID L
- InSync TITAN OPAQUE C2
- InSync ZR DENTIN D2
- InSync ZR ENAMEL 59
- InSync ZR MARGIN A4
- InSync ZR MODIFIER Light fluor.
- InSync ZR Opal 30
- MiYO TRANS SHADE A fluor.
Showing 12 of 431 declared devices.
Catalogue references include 0010, 0154, 0764, 0809, 0877, 0951.
European nomenclature codes declared: Q010699.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | CHEMICHL AG (LI) · FDA 3008383146 |
| Devices in EUDAMED | 431 |
| Country of registration | Liechtenstein |
Device-level evidence
| Devices with a numeric GTIN | 431 |
|---|---|
| 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. Chemichl AG is registered in the United States but was not found in the Canadian register.