Medizintechnik St. Egidien GmbH
DE-MF-000009064 · Germany · St. Egidien
Medizintechnik St. Egidien GmbH is registered in the European database on medical devices as a manufacturer, with 36 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 36 |
|---|
Most frequent device types declared: 077-01, 078-01, 079-01, 090-01, 092-01.
Devices declared under this manufacturer
- Uro-Tischplatte für Azurion AD7
Showing 12 of 36 declared devices.
Catalogue references include 023, 037, 074, 076, 079, 083.
European nomenclature codes declared: Z11031180, Z11039080.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 36 |
| 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 | 36 |
|---|---|
| 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. Medizintechnik St. Egidien GmbH was not found in either the U.S. or the Canadian register.