endodoctor GmbH
DE-MF-000016960 · Germany · Fridingen
endodoctor GmbH is registered in the European database on medical devices as a manufacturer, with 88 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 88 |
|---|
Most frequent device types declared: rigid endoscopes.
Among these devices, 88 are declared reusable.
Devices declared under this manufacturer
- Endodoctor endoscope
Showing 12 of 88 declared devices.
Catalogue references include AC-040293-12, ED-019060-30-2, ED-024100-0, ED-024100-30, ED-027175-70, ED-027187-0.
European nomenclature codes declared: Z12029099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 88 |
| 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 | 88 |
|---|---|
| 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. endodoctor GmbH was not found in either the U.S. or the Canadian register.