Alegro Medical GmbH
DE-MF-000026024 · Germany · Homburg
Alegro Medical GmbH is registered in the European database on medical devices as a manufacturer, with 94 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 94 |
|---|
Devices declared under this manufacturer
- ALEGRO ALGINATE T
- ALEGRO Alginate
- ALEGRO Alginate T
- ALEGRO Alnanogel
- ALEGRO Cast
- ALEGRO Starre Zinkgelbinde
- Elastus Dermasoft Hydro
- Elastus HydroCool
- Elastus HydroZink
- Elastus Zinkleimbinde kom-bi
- Elyth CoolPro 8cm x 3m
- Medenta Alginate T 8cmx5m längselastisch
Showing 12 of 94 declared devices.
Catalogue references include 10401, 34563, 56001, 63501, 71021 / 60027, 71023 / 60023.
European nomenclature codes declared: M03020299, M030299, M03020299,M030299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 94 |
| 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 | 94 |
|---|---|
| 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. Alegro Medical GmbH was not found in either the U.S. or the Canadian register.