Venner Medical (Deutschland) GmbH
DE-MF-000005934 · Germany · Dänischenhagen
Venner Medical (Deutschland) GmbH is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 3 |
|---|---|
| Class IIa | 8 |
Among these devices, 5 are declared sterile, 3 active.
Devices declared under this manufacturer
- PEGA COMBI LINE S
- PEGA PCA Infusionspumpe
- PEGA plus Infusionspumpe
- PEGA® BAG 50 ml
- PEGA® Infuse
- PEGA® Infuse BOX 100
- PEGA® POUCH 3
- PEGA® POUCH L
- PEGA® SET 50 ml
- PEGA® SPIKE
- PEGA® TUBE
Catalogue references include 10255, 10521S, 10530, 14050, 20930, 40020.
European nomenclature codes declared: A99, Z12030301, V9099, A080201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 11 |
| 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 | 9 |
|---|---|
| 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. Venner Medical (Deutschland) GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
G10 067727 0011 | issued | 2029-07-17 |