Novalung GmbH
Country not established
- Devices
- 7
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Regimes: 510(k) Registry: 510(k)
Novaport One Vascular Access Cannula Ref K112565
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 331791694
- [email protected]
- Phone
- +49713127060
Frequently asked questions
How many devices does Novalung GmbH have in the registry?
The registry currently lists 7 devices for Novalung GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Novalung GmbH's devices?
Among its 7 most recently registered devices, Novalung GmbH has devices listed in FDA 510(k) (2 devices) and FDA GUDID (5 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Novalung GmbH's devices fall under?
Among its 7 most recently registered devices, the classes recorded for Novalung GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Novalung GmbH in the registry?
The most recently registered devices listed for Novalung GmbH include NovaPort cannula, sLA Membrane Lung, NOVALUNG SURGICAL LUNG ASSIST (SLA) MEMBRANE LUNG and NOVAPORT ONE VASCULAR ACCESS CANNULA.