Ultratex GmbH
DE-MF-000005415 · Germany · Aachen
Ultratex GmbH is registered in the European database on medical devices as a manufacturer, with 27 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 27 |
|---|
Most frequent device types declared: Vliesstofhülle.
Devices declared under this manufacturer
- Einweghaube
- Vliesstoffhülle
- Vliesstofhülle
- Vliestoffhülle
Showing 12 of 27 declared devices.
Catalogue references include 101-02, 101-04, 102-02, 102-03, 103-01, 103-02.
European nomenclature codes declared: T030199, T0207.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 27 |
| 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 | 27 |
|---|---|
| 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. Ultratex GmbH was not found in either the U.S. or the Canadian register.