Basis Medical
United Statesfrom the FDA registration address FDA FEI 3038912532
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Seclusion Catheter Ref K243436
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3038912532
- Address
- 2916 N Miami Ave, Ste 621, Miami, FL, 33127
Frequently asked questions
How many devices does Basis Medical have in the registry?
The registry currently lists 1 device for Basis Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Basis Medical's devices?
Among its 1 most recently registered device, Basis Medical has devices listed in FDA 510(k) (1 device).
What risk classes do Basis Medical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Basis Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Basis Medical in the registry?
The most recently registered devices listed for Basis Medical include Seclusion Catheter.