Derungs Licht AG
CH-MF-000015827 · Switzerland · Gossau
Derungs Licht AG is registered in the European database on medical devices as a manufacturer, with 156 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 156 |
|---|
Among these devices, 156 are declared active, 5 with a measuring function.
Authorised representative in the Union: Derungs Medical GmbH.
Devices declared under this manufacturer
- AMALIA 2 B S8
- AMALIA 2 P S7
- HALUX N50-1 P SX
- Halux N30-1 P S0 Typ1
- Halux N50-3 P SX, UK
- OPTICLUX 10-1 P TX
- TRIANGO 80-1 F Battery UK
- TRIANGO Endo 100-1 C
- TRIANGO Fokus 100-3 F
- Triango 60-3 C
- Triango 80-1 F
- Triango Fokus 100-1 F
Showing 12 of 156 declared devices.
Catalogue references include D15850000, D15895000, D15925000, D16010000, D16219000, D16251000.
European nomenclature codes declared: Z129004, Z12010702, Z12010701, V0380.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | Derungs Licht AG (CH) · FDA 1000312377 |
| Devices in EUDAMED | 156 |
| Country of registration | Switzerland |
Device-level evidence
| Devices with a numeric GTIN | 156 |
|---|---|
| Found in the U.S. device database | 6 |
| Share | 3.8 % |
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. Derungs Licht AG is registered in the United States but was not found in the Canadian register.