K.H. Dewert GmbH
DE-MF-000005967 · Germany · Bielefeld
K.H. Dewert GmbH is registered in the European database on medical devices as a manufacturer, with 158 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 158 |
|---|
Among these devices, 71 are declared active.
Devices declared under this manufacturer
- 1030/H
- 2006XL/H
- 2054XL/H
- 2090E
- 2105XL/H
- 2110XLE
- 2551XL/H
- 2605XL/H
- 2800XL/H
- 2815XLE
- 2830XL/H
- 2890XLE
Showing 12 of 158 declared devices.
Catalogue references include 2054XL/H, 2090E, 2110XLE, 2551XL/H, 2605XL/H, 2815XLE.
European nomenclature codes declared: V080603.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 158 |
| 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 | 158 |
|---|---|
| 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. K.H. Dewert GmbH was not found in either the U.S. or the Canadian register.