KeproSAN®, Inh. Kurt Kempert
DE-MF-000038505 · Germany · St. Katharinen
KeproSAN®, Inh. Kurt Kempert is registered in the European database on medical devices as a manufacturer, with 135 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 135 |
|---|
Catalogue references include 22021365, 22023157/75, 22121363, 32013809, 34013869, 40021364/VB.
European nomenclature codes declared: V080302, T030502, T04010299, V0880.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 135 |
| 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 | 135 |
|---|---|
| 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. KeproSAN®, Inh. Kurt Kempert was not found in either the U.S. or the Canadian register.