Carefusion (BD)
Country not established
- Devices
- 1
What Carefusion (BD) makes
Carefusion (Bd) manufactures the BD Alaris Pump Infusion Set, a device designed for controlled administration of intravenous fluids and medications in clinical settings.
The BD Alaris Pump Infusion Set is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
BD Alaris Pump Infusion Set Ref K250325
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Carefusion (Bd) have in the registry?
The registry currently lists 1 device for Carefusion (Bd). Devices recorded under merged duplicate company entries are counted once.
Which registries list Carefusion (Bd)'s devices?
Among its 1 most recently registered device, Carefusion (Bd) has devices listed in FDA 510(k) (1 device).
What risk classes do Carefusion (Bd)'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Carefusion (Bd)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Carefusion (Bd) in the registry?
The most recently registered devices listed for Carefusion (Bd) include BD Alaris Pump Infusion Set.