Endoaccess GmbH
DE-MF-000007568 · Germany · Garbsen
Endoaccess GmbH is registered in the European database on medical devices as a manufacturer, with 302 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 190 |
|---|---|
| Class IIb | 112 |
Most frequent device types declared: Disposable Grasping Forceps\t\t, Disposable Electrical Snare\t\t, Disposable Biopsy Forceps, Disposable Injection Needle, Reusable Electrical Snare.
Among these devices, 256 are declared sterile.
No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 302 |
| Country of registration | Germany |
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.