DISCHER Technik GmbH
DE-MF-000004972 · Germany · Haan
DISCHER Technik GmbH is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 8 |
|---|
Most frequent device types declared: Master.
Among these devices, 8 are declared active.
Devices declared under this manufacturer
- DISCHER Boy
- DISCHER Boy Plus
- DISCHER Boy S
- DISCHER Compact
- DISCHER Master
- DISCHER Master S
- DISCHER Piccolo
- DISCHER Piccolo S
Catalogue references include 20204 / 20205 / 20206 / 20207, 20208 / 20209 / 20210 / 20211, 20212 / 20213, 20214 / 20215 / 20216 / 20217, 20218 / 20219, 20220.
European nomenclature codes declared: Z12011301.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 8 |
|---|---|
| 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. DISCHER Technik GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
1000308760 | supplemented | 2029-03-13 |