indoor-gruppe
DE-MF-000047869 · Germany · Chemnitz
indoor-gruppe is registered in the European database on medical devices as a manufacturer, with 12 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 12 |
|---|
Devices declared under this manufacturer
- HEA 212SP
- NM 500SP
- SRT 210SP
- SRT 211SP mit Tragegriff
- SRT 211SP ohne Tragegriff
- SRT 215SP
- Seitengitterpolster Universal
- Seitengitterpolster geteilt mit Klettband
- Seitengitterpolster geteilt mit Reißverschluss
- Seitengitterpolster mit Klettband
- Seitengitterpolster mit Reißverschluss
Catalogue references include 0930031, 0930045, 093005214HO, 0930077, 0930195, 10070020802895.
European nomenclature codes declared: V08068099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 12 |
| 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 | 12 |
|---|---|
| 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. indoor-gruppe was not found in either the U.S. or the Canadian register.