Kluge & Fielitz GmbH
DE-MF-000016427 · Germany · Neiße-Malxetal
Kluge & Fielitz GmbH is registered in the European database on medical devices as a manufacturer, with 23 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 23 |
|---|
Most frequent device types declared: KF.
Devices declared under this manufacturer
- KF 200 XL
- KF 200 XL/D
- KF 300 D/T
- KF 300 T
- KF 300 XL/D
- KF 300 XL/T
- KF 900 XL/D
- KF200 T
- KF300
- KF300 XL/D/T
- KF900 D
- KF900 D/T
Showing 12 of 23 declared devices.
Catalogue references include KF 900 XL/D/T, Waschanlage, Waschstraße.
European nomenclature codes declared: V0799, Z12011301.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 23 |
| 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 | 23 |
|---|---|
| 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. Kluge & Fielitz GmbH was not found in either the U.S. or the Canadian register.