Xpedite Diagnostics GmbH
DE-MF-000020021 · Germany · Hallbergmoos
Xpedite Diagnostics GmbH is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: EBX-079-200.
Devices declared under this manufacturer
- Releaser
- SwiftX Media
Catalogue references include EBE-078-200, EBX-079, SGP-96-IVD, SGR-25-IVD, SXD-25-IVD, SXEA-50-IVD.
European nomenclature codes declared: W0105011699,W0105050399,W0105060499,W0105070201, W0105011699,W01050499, W01050499, W0105011699,W01050499,W0105050399,W0105060499,W0105070201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| 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 | 8 |
|---|---|
| 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. Xpedite Diagnostics GmbH was not found in either the U.S. or the Canadian register.