Neoventa Medical AB
Active in EUDAMEDSwedenfrom SRN EUDAMED FDA SRN SE-MF-000001402 FEI 3004729605
- Devices
- 2
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
Goldtrace Fetal Spiral Electrode (FSE) Ref CNS000004
Regimes: CE MDR 510(k) Registry: EUDAMEDGUDIDStan S31 Fetal Heart Monitor Ref P020001
Regimes: PMA Registry: PMA
Company details
- EUDAMED SRN
- SE-MF-000001402
- FDA FEI number
- 3004729605
- DUNS number
- 776720448
- EU VAT number
- SE556773478401
- EUDAMED status
- Active
- EUDAMED registered name
- Neoventa Medical AB
- Registered address
- 32, Norra Ågatan, 43135, Mölndal, Sweden
- Website
- www.neoventa.com/
- [email protected]
- Phone
- 0046317583200
- PRRC contact
- Johan Sundberg
Frequently asked questions
How many devices does Neoventa Medical AB have in the registry?
The registry currently lists 2 devices for Neoventa Medical AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neoventa Medical AB's devices?
Among its 2 most recently registered devices, Neoventa Medical AB has devices listed in EUDAMED (1 device), FDA PMA (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Neoventa Medical AB's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Neoventa Medical AB's devices are Class IIa and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Neoventa Medical AB in the registry?
The most recently registered devices listed for Neoventa Medical AB include Goldtrace Fetal Spiral Electrode (FSE) and STAN S31 FETAL HEART MONITOR.