livetec Ingenieurbüro GmbH
DE-MF-000005598 · Germany · Lörrach
livetec Ingenieurbüro 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 | 9 |
|---|---|
| Class IIb | 5 |
Among these devices, 12 are declared active.
Devices declared under this manufacturer
- Cardioline ECG
- LASS-Expert
- Lasotronic MTL 100
- Lasotronic MTL 50
- PowerTwin21
- PowerTwin21 XP5
- VIREOFLEX3
- VIREOFLEX3 Cable Adapter
- auxil ECG
- dpv-ritmo III
- kECG-3
- kECG-3 (Kardiobeat.ai)
Showing 12 of 14 declared devices.
Catalogue references include 105898, 106869, 106871, 106895, 107152, 107153.
European nomenclature codes declared: Z12050403, Z120615, C020501.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 14 |
| 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 | 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. livetec Ingenieurbüro GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
Z-23-143-S-E | issued | 2031-02-18 |
HZ 1448989-1 | issued | 2030-10-13 |