ScheBo Biotech AG
Active in EUDAMEDGermanyfrom SRN EUDAMED FDA SRN DE-MF-000024072 FEI 3003780132
- Devices
- 6
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
What ScheBo Biotech AG makes
ScheBo Biotech AG produces in-vitro diagnostic (IVD) reagents and kits for blood sample preparation, including buffers for washing, extraction, and sample handling, as well as pre-packaged patient sets for hemoglobin testing.
These products are classified as Class A medical devices and are registered in the EU’s eudamed database. The company is based in Germany.
Catalogue
ScheBo Quick-Prep Ref 28-Quick-L
Regimes: CE IVDR Registry: EUDAMEDScheBo Hb Smart Patient Set Ref 26-P
Regimes: CE IVDR Registry: EUDAMEDSample/Washing Buffer 5x Ref 03
Regimes: CE IVDR Registry: EUDAMEDScheBo Quick-Prep XL Ref 16
Regimes: CE IVDR Registry: EUDAMEDScheBo Master Quick-Prep Ref 28-Quick
Regimes: CE IVDR Registry: EUDAMEDGUDIDScheBo Extraction Buffer Ref 02
Regimes: CE IVDR Registry: EUDAMEDGUDID
Company details
- EUDAMED SRN
- DE-MF-000024072
- FDA FEI number
- 3003780132
- EU VAT number
- DE112632803
- EUDAMED status
- Active
- EUDAMED registered name
- ScheBo Biotech AG
- Registered address
- 3-5, Netanyastr., 35394, Gießen, Germany
- Website
- www.schebo.com
- [email protected]
- Phone
- +4964149960
- PRRC contact
- Jeffrey Scheefers
Frequently asked questions
How many devices does ScheBo Biotech AG have in the registry?
The registry currently lists 6 devices for ScheBo Biotech AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list ScheBo Biotech AG's devices?
Among its 6 most recently registered devices, ScheBo Biotech AG has devices listed in EUDAMED (6 devices) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do ScheBo Biotech AG's devices fall under?
Among its 6 most recently registered devices, the classes recorded for ScheBo Biotech AG's devices are IVDR Class A. Each device page shows its own class and authorisation.
What are the newest devices from ScheBo Biotech AG in the registry?
The most recently registered devices listed for ScheBo Biotech AG include ScheBo Quick-Prep, ScheBo Hb Smart Patient Set, Sample/Washing Buffer 5x and ScheBo Quick-Prep XL.