WiMedical GmbH
DE-MF-000036069 · Germany · Singen (Hohentwiel)
WiMedical GmbH is registered in the European database on medical devices as a manufacturer, with 41 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 41 |
|---|
Most frequent device types declared: 1/1 BIG-Deckel-Drahtsieb, 1/1-Deckel-Drahtsieb, 1/1-Deckel-Edelstahl, 1/1-Deckel-Hybrid, 106er-1/1-BIG-Boden-FG-Drahtsieb.
Among these devices, 40 are declared reusable.
Devices declared under this manufacturer
- 1/1 BIG-Deckel-Drahtsieb
- 1/1-Deckel-Drahtsieb
- 1/1-Deckel-Edelstahl
- 1/1-Deckel-Hybrid
- 1/2-Deckel-Edelstahl
- 106er-1/1-BIG-Boden-FG-Drahtsieb
- 106er-1/2-Boden-FG-Drahtsieb
- 106er-1/2-Boden-FG-Edelstahl
- 56er-1/1-BIG-Boden-FG-Drahtsieb
- 56er-1/1-Boden-FG-Hybrid
- 56er-1/2-Boden-FG-Drahtsieb
- 56er-1/2-Boden-FG-Edelstahl
Showing 12 of 41 declared devices.
Catalogue references include DS-11000-0, DS-12004-1, DSB-11004-1, DSB-11008-1, ES-11000-0, ES-12004-1.
European nomenclature codes declared: S010401.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 41 |
| 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 | 41 |
|---|---|
| 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. WiMedical GmbH was not found in either the U.S. or the Canadian register.