VTI Ventil Technik GmbH
DE-MF-000006534 · Germany · Iserlohn
VTI Ventil Technik GmbH is registered in the European database on medical devices as a manufacturer, with 53 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 49 |
|---|---|
| Class IIa | 4 |
Most frequent device types declared: K622-Serie, K623-Serie, K666-Serie.
Among these devices, 31 are declared active.
Devices declared under this manufacturer
- MediLight
Showing 12 of 53 declared devices.
Catalogue references include 622210D03-S160, 622241D01-S63, 622241PX01-S26, 622241PX01-S66, 622340D01-S241, 622341D01-S102.
European nomenclature codes declared: R9080.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 53 |
| 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 | 53 |
|---|---|
| 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. VTI Ventil Technik GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
1332GB448260528 | amended | 2028-06-10 |