Univent Medical GmbH
DE-MF-000015594 · Germany · Villingen Schwenningen
Univent Medical GmbH is registered in the European database on medical devices as a manufacturer, with 32 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 32 |
|---|
Devices declared under this manufacturer
- ONEHIIRO ALLERGY PRO MAX / 10 Masken einzeln verpackt
- ONEHIIRO PRO MAX / 10 Masken einzeln verpackt
- ONEHIIRO PRO MAX / 10 Masken im Beutel
- ONEHIIRO PRO MAX / 5 Masken im Beutel
- ONEHIIRO PRO MINI / 10 Masken einzeln verpackt
- ONEHIIRO PRO MINI / 5 Masken im Beutel
- atemious pro2+ / 10 Masken einzeln verpackt
- atemious pro2+ / 30 Masken einzeln verpackt
- atemious pro2XXS+
- atemious pro2XXS+ / 30 Masken einzeln verpackt
- atemious pro2XXS+ / 30 Masken im Beutel
- atemious pro5+ / 10 Masken einzeln verpackt
Showing 12 of 32 declared devices.
Catalogue references include 0001 - 005, 0001 - 011, 0003 - 005, 0013 - 011, 2103, 2104.
European nomenclature codes declared: T020604.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 32 |
| 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 | 32 |
|---|---|
| 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. Univent Medical GmbH was not found in either the U.S. or the Canadian register.