Reinecker Vision GmbH
DE-MF-000025998 · Germany · Alsbach-Hähnlein
Reinecker Vision GmbH is registered in the European database on medical devices as a manufacturer, with 51 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 51 |
|---|
Among these devices, 51 are declared active.
Devices declared under this manufacturer
- MANO 12 V1.0
- MANO 12 V2.0
- MANO EDU lite
- Mano XL
- VEO VOX mit Touchscreen 24\
- VERDE Videomatic 20
- VERDE Videomatic 22
- VERDE mezzo 01
- VERDE mezzo 20
- VOX box pro V4.0
- Videomatic 20
- Videomatic 24
Showing 12 of 51 declared devices.
Catalogue references include MANEDLI1, MEZEDU01, MEZZO2K1, VEOVO241, VERMEZ20, VERVM201.
European nomenclature codes declared: V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 51 |
| 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 | 51 |
|---|---|
| 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. Reinecker Vision GmbH was not found in either the U.S. or the Canadian register.