Diagnostic Green GmbH
Active in EUDAMEDGermanyfrom SRN EUDAMED FDA SRN DE-MF-000017068 FEI 3042243691
- Devices
- 2
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
What Diagnostic Green GmbH makes
Diagnostic Green GmbH makes the IC-Flow Imaging System 2.0 and IC-Flow 2, which are imaging systems used for diagnostic purposes.
The company's devices are classified as Class I and Class II medical devices and are listed in the EUDAMED and FDA 510(k) registries. Diagnostic Green GmbH is based in Germany.
Catalogue
IC-Flow™ Imaging System 2.0 Ref K243645
Regimes: CE MDR 510(k) Registry: 510(k)IC-Flow 2 Ref PC6300
Regimes: CE MDR Registry: EUDAMED
Company details
- EUDAMED SRN
- DE-MF-000017068
- FDA FEI number
- 3042243691
- EU VAT number
- DE299617548
- EUDAMED status
- Active
- EUDAMED registered name
- Diagnostic Green GmbH
- Registered address
- 7c, Feldkirchener Str., 85551, Kirchheim b. München, Germany
- [email protected]
- PRRC contact
- Stefan Bolleininger
Frequently asked questions
How many devices does Diagnostic Green GmbH have in the registry?
The registry currently lists 2 devices for Diagnostic Green GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diagnostic Green GmbH's devices?
Among its 2 most recently registered devices, Diagnostic Green GmbH has devices listed in EUDAMED (1 device) and FDA 510(k) (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Diagnostic Green GmbH's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Diagnostic Green GmbH's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Diagnostic Green GmbH in the registry?
The most recently registered devices listed for Diagnostic Green GmbH include IC-Flow™ Imaging System 2.0 and IC-Flow 2.