Dietz Power B.V.
NL-MF-000010827 · Netherlands · Helmond
Dietz Power B.V. is registered in the European database on medical devices as a manufacturer, with 17 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 17 |
|---|
Most frequent device types declared: (x)xl, advanced, slimline.
Among these devices, 17 are declared active.
Devices declared under this manufacturer
- SANGO advanced FWD SEGO
- SANGO advanced FWD SEGO basic
- SANGO advanced FWD SEGO junior
- SANGO advanced MWD SEGO
- SANGO advanced MWD SEGO basic
- SANGO advanced MWD SEGO junior
- SANGO advanced RWD SEGO
- SANGO advanced RWD SEGO basic
- SANGO slimline FWD SEGO junior
- SANGO slimline MWD SEGO
- SANGO slimline RWD SEGO
- SANGO slimline RWD SEGO junior
Showing 12 of 17 declared devices.
Catalogue references include SANGO advanced FWD SEGO basic, SANGO advanced MWD SEGO, SANGO advanced RWD SEGO, SANGO advanced RWD SEGO basic, SANGO slimline FWD SEGO junior, SANGO slimline MWD SEGO.
European nomenclature codes declared: Y122127.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 17 |
| Country of registration | Netherlands |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 17 |
|---|---|
| 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. Dietz Power B.V. was not found in either the U.S. or the Canadian register.