ENDO-PASSION GmbH
DE-MF-000010700 · Germany · Wurmlingen
ENDO-PASSION GmbH is registered in the European database on medical devices as a manufacturer, with 20 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 20 |
|---|
Most frequent device types declared: Flexible Biopsiezange Gastroenterologie, Zange, Greif, flexible Endoskopie.
Among these devices, 20 are declared reusable.
Devices declared under this manufacturer
- Biopsiezangen für die Gastroenterologie
- Fremdkörper-Fasszange
- Frendkörper-Fasszange
Showing 12 of 20 declared devices.
Catalogue references include 1117RVr-180, 1117RVso-180, 1134RVr-230, 11D23RVlo-180, 1623RV-180, 1623RV-230.
European nomenclature codes declared: G0399, G03050199.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | ENDO-PASSION GMBH (DE) · FDA 3011398162 |
| Devices in EUDAMED | 20 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 20 |
|---|---|
| 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: United States only. ENDO-PASSION GmbH is registered in the United States but was not found in the Canadian register.