Rein medical GmbH
DE-MF-000018721 · Germany · Mönchengladbach
Rein medical GmbH is registered in the European database on medical devices as a manufacturer, with 214 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 214 |
|---|
Most frequent device types declared: All-in-One Computer, PC, Video-Monitor, WS-Video-Monitor mit PC-Option, Wall System Monitor.
Among these devices, 214 are declared active.
Devices declared under this manufacturer
- CLINIO 427DS.1
- OPERION 324 Control Panel
- OPERION 342 (SLIM)
- OPERION 346
- OPERION 349 ULTRA DUAL VIEW
- OR VIEWPORT 46\
- ORigami 46
- ORigami 49 UHD DUAL VIEW
- ORigami 55 UHD
- SILENIO 142DS
- SILENIO D155 ULTRA
- TEGRIS TOUCH 22 NON-VARIOP
Showing 12 of 214 declared devices.
Catalogue references include MAQTT02-Z, OP-324CP, OP-346, OP-349.4-HT, ST-349.4, ST-35U.
European nomenclature codes declared: V9099.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | REIN MEDICAL GMBH (DE) · FDA 3021071743 |
| Devices in EUDAMED | 214 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 214 |
|---|---|
| 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. Rein medical GmbH is registered in the United States but was not found in the Canadian register.