MTG GmbH
DE-MF-000005862 · Germany · Sulzbach
MTG GmbH is registered in the European database on medical devices as a manufacturer, with 17 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 8 |
|---|---|
| Class IIb | 9 |
Most frequent device types declared: Cura-H, Cura-V, Geräteschiene GS2 Halterabstand 40 cm, Ligno-H, Ligno-V.
Among these devices, 9 are declared active.
Devices declared under this manufacturer
- Cura-H
- Cura-V
- Geräteschiene GS2 Halterabstand 40 cm
- Halterung Space 1-fach
- Halterung Spaceplus 1-fach
- Ligno-H
- Ligno-V
- Optima
- Sechsfachsteckdosenleiste
- Sechsfachsteckdosenleiste mit 12 Feinsicherungen (Jede Steckdose ist e
- Verso
- Verso-OP
Showing 12 of 17 declared devices.
Catalogue references include 12100, 17202, 17205, 30010, 30020, 30060.
European nomenclature codes declared: Z129017, Z129099, Z12030380, V9099, Z120309.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 17 |
| 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 | 17 |
|---|---|
| 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. MTG GmbH was not found in either the U.S. or the Canadian register.