Oehm und Rehbein GmbH
FDA registration: Germany Last updated 30 May 2026 Part of Oehm Und Rehbein GmbH
- Devices
- 6
- Registries
- GUDIDFDA
- FDA recalls
- 0
Catalogue
dicomPACS®DX-R 4.3 Ref 4.3
dicomPACS®DX-R 5 Ref 5
Amadeo M-DR mini Ref Amadeo M-DR mini with Varex flat panel detector
dicomPACS 8.3 Ref 8.3
Amadeo M-DR mini Amadeo M-AX Ref Amadeo M-AX
Amadeo M-DR mini with XenOR flat panel Ref Amadeo M-DR mini with XenOR flat panel
FDA establishments
- Oehm Und Rehbein GmbH ROSTOCK Mecklenburg-Western Pomerania · DE FEI 3006542593
Frequently asked questions
How many devices does Oehm und Rehbein GmbH have in the registry?
The registry currently lists 6 devices for Oehm und Rehbein GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oehm und Rehbein GmbH's devices?
Among its 6 most recently registered devices, Oehm und Rehbein GmbH has devices listed in FDA GUDID (6 devices).
What risk classes do Oehm und Rehbein GmbH's devices fall under?
Among its 6 most recently registered devices, the classes recorded for Oehm und Rehbein GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oehm und Rehbein GmbH in the registry?
The most recently registered devices listed for Oehm und Rehbein GmbH include dicomPACS®DX-R 4.3, dicomPACS®DX-R 5, Amadeo M-DR mini and dicomPACS 8.3.
Which FDA establishments are linked to Oehm und Rehbein GmbH?
1 FDA establishment is linked to Oehm und Rehbein GmbH in the registry; they are listed on the company page.
Information
- FDA registration
- Germany
- DUNS number
- 344349290