Cardionovum GmbH
DE-MF-000005316 · Germany · Bonn
Cardionovum GmbH is registered in the European database on medical devices as a manufacturer, with 28 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 28 |
|---|
Among these devices, 28 are declared sterile.
Devices declared under this manufacturer
- RESTORE BEB
- RESTORE DEB
Showing 12 of 28 declared devices.
Catalogue references include R 2.25-25, R 2.50-20, R 2.75-20, R 2.75-25, R 4.00-15, R 4.00-20.
European nomenclature codes declared: C010401020101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 28 |
| 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 | 28 |
|---|---|
| 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. Cardionovum GmbH was not found in either the U.S. or the Canadian register.