HomeBraceGermany GmbH
DE-MF-000015606 · Germany · Urbach
HomeBraceGermany GmbH is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 6 |
|---|
Among these devices, 6 are declared active.
Devices declared under this manufacturer
- MyEcc Control
- MyEcc Prop
- MyEcc Pupil
- MyEcc Pupil Prop
- MyEcc V5
- MyEnvi
Catalogue references include 10226, 10326, 10333, 10433, 10434, 10467.
European nomenclature codes declared: Y99, Y241299.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | HomeBraceGermany GmbH (DE) · FDA 3038289351 |
| Devices in EUDAMED | 6 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 6 |
|---|---|
| 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: United States only. HomeBraceGermany GmbH is registered in the United States but was not found in the Canadian register.