i3 Membrane GmbH
Active in EUDAMEDGermanyfrom SRN EUDAMED FDA SRN DE-MF-000007284 FEI 3022699154
- Devices
- 6
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Regimes: CE MDR 510(k) Registry: EUDAMED510(k)
i3 TWO direct Ref 203300
Regimes: CE MDR Registry: EUDAMEDi3 TWO connect Ref 203200
Regimes: CE MDR Registry: EUDAMED
Company details
- EUDAMED SRN
- DE-MF-000007284
- FDA FEI number
- 3022699154
- DUNS number
- 312843892
- EUDAMED status
- Active
- EUDAMED registered name
- i3 Membrane GmbH
- EUDAMED abbreviated name
- i3 Membrane
- Registered address
- 1, Christoph-Seydel-Straße, 01454, Radeberg, Germany
- Website
- www.i3membrane.de
- [email protected]
- Phone
- +494025767480
- PRRC contact
- Hauke Tammena
Frequently asked questions
How many devices does i3 Membrane GmbH have in the registry?
The registry currently lists 6 devices for i3 Membrane GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list i3 Membrane GmbH's devices?
Among its 6 most recently registered devices, i3 Membrane GmbH has devices listed in EUDAMED (3 devices), FDA 510(k) (1 device) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do i3 Membrane GmbH's devices fall under?
Among its 6 most recently registered devices, the classes recorded for i3 Membrane GmbH's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from i3 Membrane GmbH in the registry?
The most recently registered devices listed for i3 Membrane GmbH include i3 ONE 203100-S, i3 TWO connect 203200-S, i3 TWO direct 203300-S and i3 ONE (203100-S);i3 TWO connect (203200-S);i3 TWO direct (203300-S).