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 Biopsy Forceps, Disposable Cleaning Brush, Disposable Electrical Forceps\t\t, Disposable Electrical Knife\t, Disposable Electrical Snare\t\t.
Among these devices, 256 are declared sterile.
Devices declared under this manufacturer
- Disposable Biopsy Forceps
- Disposable Cleaning Brush
- Disposable Cytology Brush
- Disposable Cytology Brush\t\t
- Disposable Electrical Forceps\t\t
- Disposable Electrical Knife\t
- Disposable Electrical Snare\t\t
- Disposable Grasping Forceps\t\t
- Disposable Injection Needle
- Disposable Spray Catheter\t\t
- Disposable Valve Cap
- Disposable Valve Caps
Showing 12 of 302 declared devices.
Catalogue references include EA-S18AG16, EA-S18PG10, EA-S18SN10, EA-S18SN16, EA-S24OS2330, EA-S24OSN2115.
European nomenclature codes declared: G03030102, G03050199, G0308010101, G03020101, G030899, V070102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 302 |
| 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 | 302 |
|---|---|
| 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. Endoaccess GmbH was not found in either the U.S. or the Canadian register.