Solabia Xebios GmbH
DE-MF-000054384 · Germany · Düsseldorf
Solabia Xebios GmbH is registered in the European database on medical devices as a manufacturer, with 532 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- Brain heart infusion broth
- CHROMagar™ ESBL
- Carbohydrate, mannitol phenolred-peptonewater
- DNA'se test agar
- Fastidious anaerobe agar + 5% horseblood (EUCAST)
- GC Agar + Haemoglobine + vitox
- GC agar + vitox
- Legionella agar without cysteïn
- NAT Medium 1
- Sabouraud dextrose agar
- Selenite broth
- TB-medium with pyruvate/PACT (slanted)
Showing 12 of 532 declared devices.
Catalogue references include 11.0017, 11.0408, 11.0431, 11.1718, 11.1986, 21.0283.
European nomenclature codes declared: W0104010405, W0104010206, W0104010306, W0104030201, W0104030301, W0104010407.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 532 |
| 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 | 532 |
|---|---|
| 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. Solabia Xebios GmbH was not found in either the U.S. or the Canadian register.