Bdh, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Bdh, Inc. makes
Bdh, Inc. manufactures haemodialysis concentrate used in renal replacement therapy.
The company is based in the US, and its products are regulated as Class II medical devices listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Haemodialysis Concentrate Ref K904946
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bdh, Inc. have in the registry?
The registry currently lists 1 device for Bdh, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bdh, Inc.'s devices?
Among its 1 most recently registered device, Bdh, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Bdh, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bdh, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bdh, Inc. in the registry?
The most recently registered devices listed for Bdh, Inc. include HAEMODIALYSIS CONCENTRATE.