Besco Medical Medizin- und Rehaprodukte GmbH
DE-MF-000008152 · Germany · Kronau
Besco Medical Medizin- und Rehaprodukte GmbH is registered in the European database on medical devices as a manufacturer, with 90 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 90 |
|---|
Among these devices, 1 are declared active.
Devices declared under this manufacturer
- Compact bordeaux
- MOBILITYPlus+ RIO SB40
- MOBILITYPlus+ RIO SB50
- MobilityPlus+ IR10+ red
- MobilityPlus+ IR10+ white
- Primus ML 2.0 SB43+C
- Primus ML 2.0 SB48
- Primus ML 2.0 SB50+DB
- Spring Medium bordeaux
- Spring Medium cappuccino
- Spring Small bordeaux
- Spring Small graphit
Showing 12 of 90 declared devices.
Catalogue references include 2148170, 2950120, 4260685531084, 6956410, 7249670, 7249870.
European nomenclature codes declared: Y122106, Y120606, T020604, Y122410, T020603.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 90 |
| 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 | 90 |
|---|---|
| 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. Besco Medical Medizin- und Rehaprodukte GmbH was not found in either the U.S. or the Canadian register.