BD/Preefil
Country not established
- Devices
- 1
What BD/Preefil makes
The company manufactures prefilled saline flush syringes designed for intravenous use, including the BD PreeFIL Normal Saline Flush Syringe.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bd/Preefil have in the registry?
The registry currently lists 1 device for Bd/Preefil. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bd/Preefil's devices?
Among its 1 most recently registered device, Bd/Preefil has devices listed in FDA 510(k) (1 device).
What risk classes do Bd/Preefil's devices fall under?
Among its 1 most recently registered device, the classes recorded for Bd/Preefil's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bd/Preefil in the registry?
The most recently registered devices listed for Bd/Preefil include BD PREEFILE NORMAL SALINE FLUSH SYRINGE FLUSH SYRINGE.