ScheBo Biotech AG
DE-MF-000024072 · Germany · Gießen
ScheBo Biotech AG is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
Devices declared under this manufacturer
- Sample/Washing Buffer 5x
- ScheBo Extraction Buffer
- ScheBo Master Quick-Prep
- ScheBo Quick-Prep
- ScheBo Quick-Prep XL
Catalogue references include 02, 03, 16, 26-P, 28-Quick, 28-Quick-L.
European nomenclature codes declared: W05019001, W01029003.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | SCHEBO BIOTECH AG (DE) · FDA 9614972 |
| Devices in EUDAMED | 6 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 6 |
|---|---|
| Found in the U.S. device database | 2 |
| Share | 33.3 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | SCHEBO BIOTECH AG |
North American profile: Both markets. ScheBo Biotech AG is registered in both the United States and Canada.