EndoMed Systems GmbH
DE-MF-000015581 · Germany · Ravensburg
EndoMed Systems GmbH is registered in the European database on medical devices as a manufacturer, with 53 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 44 |
|---|---|
| Class IIb | 9 |
Most frequent device types declared: Arthroscope, COMBO 3 Gastroscope G34Q / COMBO 3 Gastroscope G34 / COMBO 3 Colonosco, COMBO 3 Processor P34, Cystoscope, ENDO Pump 200D / ENDO Pump 100 / ENDO Pump 100 Arthroscopy Pump / ENDO.
Among these devices, 37 are declared reusable, 16 active, 15 with a measuring function.
Devices declared under this manufacturer
- EndoMed System GmbH
- EndoMed Systems GmbH
Showing 12 of 53 declared devices.
Catalogue references include 810230, 811101, 811142, 821001, 821003, 821009.
European nomenclature codes declared: Z12021101, Z12029009, Z12020704, Z12029008, L030101, Z12020701.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 53 |
| 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 | 53 |
|---|---|
| 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. EndoMed Systems GmbH was not found in either the U.S. or the Canadian register.