MAG & More GmbH
DE-MF-000012125 · Germany · München
MAG & More GmbH is registered in the European database on medical devices as a manufacturer, with 38 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 38 |
|---|
Most frequent device types declared: Apollo TMS Therapy System, PowerMAG, Stimulation Coils, Stimware.
Among these devices, 38 are declared active.
Devices declared under this manufacturer
- Apollo TMS Therapy System 100 V
- Apollo TMS Therapy System 220 V
- HANS-aCool
- PMR110
- PowerMAG Clinical 100 (220 V)
- PowerMAG Clinical 30 (220 V)
- PowerMAG Clinical 30 (230 V)
- PowerMAG Research 100 (220 V)
- PowerMAG Research 100 ppTMS (220 V)
- Stimware
- Stimware FDA
- Stimware TBS EMG AutoMT
Showing 12 of 38 declared devices.
Catalogue references include 112249, 112250, 112279, 112289, 150601, 150643.
European nomenclature codes declared: Z12101105.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | MAG & MORE GMBH (DE) · FDA 3012823347 |
| Devices in EUDAMED | 38 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 38 |
|---|---|
| Found in the U.S. device database | 1 |
| Share | 2.6 % |
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: United States only. MAG & More GmbH is registered in the United States but was not found in the Canadian register.