Oxoid Deutschland GmbH
DE-MF-000025401 · Germany · Wesel
Oxoid Deutschland GmbH is registered in the European database on medical devices as a manufacturer, with 101 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- 7% SHEEP BLOOD AGAR WITH GENTAMICIN
- BRILLIANCE UTI CLARITY
- COLUMBIA AGAR WITH SHEEP BLOOD
- COLUMBIA AGAR WITH SHEEP BLOOD PLUS/ MACCONKEY AGAR W/O SALT
- COLUMBIA AGAR+SB PLUS/SCHOKO-AGAR+SB
- COLUMBIA CAP SELECTIVE AGAR WITH SHEEP BLOOD
- DRIGALSKI-LACTOSE AGAR
- HAEMOPHILUS SELECTIVE AGAR
- MANNITOL SALT AGAR
- MUELLER-HINTON-AGAR
- NUTRIENT BROTH WITH GLUCOSE
- PSEUDOMONAS CFC SELECTIVE MEDIUM
Showing 12 of 101 declared devices.
Catalogue references include PB5008A, PB5186A, PB5254E, PO5097A, PO5159A, PO5167A.
European nomenclature codes declared: W0104010405, W0104010206, W0104010407, W0104030201, W0104010403, W0104030301.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 101 |
| 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 | 101 |
|---|---|
| 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. Oxoid Deutschland GmbH was not found in either the U.S. or the Canadian register.