Orpedo GmbH
DE-MF-000053674 · Germany · Berlin
Orpedo GmbH is registered in the European database on medical devices as a manufacturer, with 24 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 24 |
|---|
Most frequent device types declared: Cervicalstütze, Claviculabandage, Daumensattelgelenk-Orthese, Knie-Orthese, Schwangerschafts-Gurt.
Among these devices, 24 are declared active.
Devices declared under this manufacturer
- ACHILLOVIT COMP 670
- AIR WALKER PEDIVIT 605 Kurz
- AIR WALKER PEDIVIT 606
- CERVIPOL SOFT 500
- EPIVIT COMP 620
- GENUVIT COMFORT 310
- GENUVIT FIX 300
- GENUVIT STABIL 320
- HUMEROVIT 370
- LUMBOVIT DORSAL 400
- LUMBOVIT STABIL 350
- MANU POLLICIVIT 435
Showing 12 of 24 declared devices.
Catalogue references include 108-102-11-2, 108-102-11-3, 318-435, 408-508, 411-400, 428-350.
European nomenclature codes declared: Y060312, Y06120601, Y060308, Y061209, Y060612, M030501,Y060303.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 24 |
| 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 | 24 |
|---|---|
| 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. Orpedo GmbH was not found in either the U.S. or the Canadian register.