Mosler Stuntebeck Müller GbR
DE-MF-000009210 · Germany · Duderstadt
Mosler Stuntebeck Müller GbR is registered in the European database on medical devices as a manufacturer, with 33 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 33 |
|---|
Devices declared under this manufacturer
- GEO
- IO
Showing 12 of 33 declared devices.
Catalogue references include GEO_02_02_CB1, IO_01_107CM_R, IO_01_127CM_R, IO_01_152CM_L, IO_01_152CM_R, IO_01_157CM_R.
European nomenclature codes declared: Y120303.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 33 |
| 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 | 33 |
|---|---|
| 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. Mosler Stuntebeck Müller GbR was not found in either the U.S. or the Canadian register.