BioGX B.V.
Inactive in EUDAMED since 2026Netherlandsfrom SRN EUDAMED SRN NL-MF-000031736
Inactive. This company's EUDAMED actor record is marked inactive. Check the current status before ordering.
- Devices
- 1
- Registrations
- EUDAMED
At a glance
Market reach
- European Union
- EUDAMED actor
What BioGX B.V. makes
BioGX B.V. manufactures in vitro diagnostic (IVD) reagents, specifically the BioGX Syphilis test designed for use with the BD MAX system. This product is intended for detecting syphilis antibodies in clinical samples, supporting rapid diagnostic workflows in laboratory settings.
The company’s IVD products fall under Class B (General) under EU regulations and are registered in the EU’s eudamed database. BioGX B.V. is based in the Netherlands.
Catalogue
BioGX Syphilis - OSR for BD MAX Ref 400-038-C-MAX
Regimes: CE IVDD, withdrawn Registry: EUDAMED
Company details
- EUDAMED SRN
- NL-MF-000031736
- EU VAT number
- 857333094B01
- EUDAMED status
- Inactive since 2026
- EUDAMED registered name
- BioGX B.V.
- Registered address
- 408, Science Park, 1098 XH, Amsterdam, Netherlands
- Website
- www.biogx.com
- linkedin.com/company/biogx
- [email protected]
- Phone
- +12052508055
- PRRC contact
- Katharina Stein
Frequently asked questions
How many devices does BioGX B.V. have in the registry?
The registry currently lists 1 device for BioGX B.V.. Devices recorded under merged duplicate company entries are counted once.
Which registries list BioGX B.V.'s devices?
Among its 1 most recently registered device, BioGX B.V. has devices listed in EUDAMED (1 device).
What risk classes do BioGX B.V.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for BioGX B.V.'s devices are IVD general. Each device page shows its own class and authorisation.
What are the newest devices from BioGX B.V. in the registry?
The most recently registered devices listed for BioGX B.V. include BioGX Syphilis - OSR for BD MAX.