Rud Riester GmbH & CO KG
GermanyFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Minimus I; Minimus Iii, Sanaphon Ref K942649
Regimes: 510(k) Registry: 510(k)Various Stethoscopes Ref K944337
Regimes: 510(k) Registry: 510(k)Various Types Of Mercurials Ref K943461
Regimes: 510(k) Registry: 510(k)Big Ben Ref K942650
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rud Riester GmbH & CO KG have in the registry?
The registry currently lists 4 devices for Rud Riester GmbH & CO KG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rud Riester GmbH & CO KG's devices?
Among its 4 most recently registered devices, Rud Riester GmbH & CO KG has devices listed in FDA 510(k) (4 devices).
What risk classes do Rud Riester GmbH & CO KG's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Rud Riester GmbH & CO KG's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rud Riester GmbH & CO KG in the registry?
The most recently registered devices listed for Rud Riester GmbH & CO KG include MINIMUS I; MINIMUS III, SANAPHON, VARIOUS STETHOSCOPES, VARIOUS TYPES OF MERCURIALS and BIG BEN.