The Ruhof Corporation
Active in EUDAMEDAlso registered as The Ruhof Corp.
United Statesfrom SRN EUDAMED FDA SRN US-MF-000021673 FEI 3003207991
- Devices
- 1
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Scopevalet Disposable Biopsy Valve Ref K122417
Regimes: 510(k) Registry: 510(k)
Company details
- EUDAMED SRN
- US-MF-000021673
- FDA FEI number
- 3003207991
- EUDAMED status
- Active
- EUDAMED registered name
- The Ruhof Corporation
- Registered address
- 393, Sagamore Avenue, NY 11501, New York, United States
- Website
- www.ruhof.com/
- [email protected]
- Phone
- +15162945888
- PRRC contact
- Marc Esquenet
Frequently asked questions
How many devices does The Ruhof Corporation have in the registry?
The registry currently lists 1 device for The Ruhof Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Ruhof Corporation's devices?
Among its 1 most recently registered device, The Ruhof Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do The Ruhof Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for The Ruhof Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Ruhof Corporation in the registry?
The most recently registered devices listed for The Ruhof Corporation include SCOPEVALET DISPOSABLE BIOPSY VALVE.