contextflow GmbH
AT-MF-000001773 · Austria · Vienna
contextflow GmbH is registered in the European database on medical devices as a manufacturer, with 14 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 14 |
|---|
Most frequent device types declared: ADVANCE Chest CT.
Among these devices, 14 are declared active.
Devices declared under this manufacturer
- contextflow ADVANCE Chest CT
- contextflow SEARCH Lung CT
- contextflow SERACH Lung CT
Showing 12 of 14 declared devices.
Catalogue references include 3.1, 3.3.0, 4.0, contextflow ADVANCE Chest CT 2.2, contextflow SEARCH Lung CT 1.4, contextflow SERACH Lung CT 1.1.0.
European nomenclature codes declared: Z11030582, Z11030692.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 14 |
| Country of registration | Austria |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 14 |
|---|---|
| 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. contextflow GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
G10 103663 0002 | issued | 2026-06-06 |