MESA Medizintechnik GmbH
DE-MF-000006808 · Germany · Benediktbeuern
MESA Medizintechnik GmbH is registered in the European database on medical devices as a manufacturer, with 25 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 25 |
|---|
Most frequent device types declared: Patiendata-Management-Software-System.
Among these devices, 1 are declared active.
Devices declared under this manufacturer
- DDC digital Diagnostic Center
Showing 12 of 25 declared devices.
Catalogue references include ADK-101450, ADK-121530, ADK-121550, ADK-901530, DIA-401060.3, DIA-701288.3.
European nomenclature codes declared: V9099, V92.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 25 |
| 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 | 25 |
|---|---|
| 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. MESA Medizintechnik GmbH was not found in either the U.S. or the Canadian register.